Alkenone-based formulations for topical applications

ABSTRACT

The use of long-chain alkenones to impart desired characteristics in personal care compositions for topical applications is described. The preparation of mixtures long-chain alkenones and synthetic derivatives thereof is presented. Examples of compositions include abrasive soaps, with alkenones serving as natural exfoliating agents. Alkenones and their derivatives can serve as emollients, occlusive agents, encapsulating agents, stabilizing agents, binding agents, thickening agents, surfactants, and antimicrobials.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims the benefit of U.S. patent application No.62/255,961, filed Nov. 16, 2015, the disclosure of which is herebyincorporated by reference in its entirety.

BACKGROUND

Many consumer products rely on petroleum-derived compounds to providethe necessary properties for their intended use. However, with growinghealth and environmental concerns about the use of petrochemicals, thereis a need for alternative compounds from renewable and sustainablesources. For example, plastic-exfoliating beads have been recentlybanned in some states. See, e.g., Abrams, R., “Fighting Pollution fromMicrobeads Used in Soaps and Creams,” New York Times, May 22, 2015.

Abrasives are common to a variety of cleansers (e.g., body washes,facial cleansers, etc.) because they can produce a softer skin feel, andare typically made from polymers such as polyethylene, apetroleum-derived material. Widespread daily use of these products hasproduced an enormous accumulation and persistence of polymeric abrasivesin the marine and fresh water environment whose impact, to even humanhealth, is only recently becoming appreciated. See, e.g., Yang, D. etal., “Microplastic Pollution in Table Salts from China,” Environ. Sci.Tech. 2015, 49, pp 13622-13627, DOI: 10.1021/acs.est.5b03163. Replacingmicroplastics of this type while maintaining quality is, however,challenging, as other natural or biodegradable ingredients such asground fruit pits and nut shells fail to match the smoothness ofpolyethylene beads, resulting in increased skin damage.

Algae are highly prized as rich and diverse sources of various renewablehigh-value chemicals. One example is within the omega-3 polyunsaturatedfatty acid (“PUFA”) market. In 2012, the global market for microalgaedocosahexaenoic acid (DHA), an essential omega-3, a PUFA that has beentied to brain health, was estimated to be $350 million and about 4,600metric tons. See, e.g., Shanahan, C., “The global algae oil omega-3market in 2014,” Algae Industry Magazine.com, May 18, 2014. Infantformula applications represented nearly half of the microalgae-based DHAmarket, followed by dietary supplements and food/beverages.

Benefits of algae-derived chemicals include the ability of some algae togrow in brackish water, salt water, or wastewater, or on otherwisenon-arable land, thus not competing for water or land resources. Asphotosynthetic organisms, algae also fix CO₂, thereby decreasingatmospheric concentrations of this problematic greenhouse gas whencompared to burning petroleum fuels. Additionally, unlike traditionalagricultural crops, the use of algae to make non-food products would notaffect food supplies and prices.

Accordingly, there is a need for replacement of petroleum-derivedcompounds with compounds from renewable sources. The present disclosureseeks to fulfill these needs and provides related advantages.

SUMMARY

This summary is provided to introduce a selection of concepts in asimplified form that are further described below in the DetailedDescription. This summary is not intended to identify key features ofthe claimed subject matter, nor is it intended to be used as an aid indetermining the scope of the claimed subject matter.

In one aspect, the present disclosure provides, inter alia, a personalcare composition, including:

a compound of Formula (I):

wherein

R₁ is methyl or ethyl; and

R₂ is a C₃₀₋₄₅ alkenyl having at least one trans double carbon-carbonbond, or R₂ is a C₃₀₋₄₅ alkyl;

provided that the compound of Formula (I) is not

In another aspect, the present disclosure provides, inter alia, apersonal care composition, including:

at least one compound of Formula (II), Formula (III), or Formula (IV):

wherein

R₃ is selected from —OH, —O(CH₂CH₂)_(n)OSO₃—, and —O(CH₂)(CHOH)(CHOH),

-   -   wherein n is an integer of from 1 to 200, and

R₂ is a C₃₀₋₄₅ alkenyl having at least one trans double carbon-carbonbond, or R₂ is a C₃₀₋₄₅ alkyl;

wherein

R₁ is methyl or ethyl;

R₂ is a C₃₀₋₄₅ alkenyl having at least one trans double carbon-carbonbond, or R₂ is a C₃₀₋₄₅ alkyl;

R₄, R₅, and R₆ are each independently selected from H, C₁₋₆ alkyl, C₁₋₆haloalkyl, and halo; and

R₇ is selected from H and —CO₂—;

wherein

R₁ is methyl or ethyl;

R₂ is a C₃₀₋₄₅ alkenyl having at least one trans double carbon-carbonbond, or R₂ is a C₃₀₋₄₅ alkyl;

R₈ is selected from —SO₃—, —PO₂—OR₉, and —CONHR₁₀,

-   -   wherein R₉ is —CH₂CH₂N⁺R₁₁R₁₂R₁₃, wherein R₁₁, R₁₂, and R₁₃ are        each independently selected from H, C₁₋₆ alkyl, C₁₋₆ haloalkyl,        and halo, and    -   R₁₀ is —(CH₂)_(m)SO₃—, —(CH₂)_(m)N⁺R₁₄R₁₅CH₂CO₂—,        —(CH₂)_(m)N⁺R₁₆R₁₇R₁₈,        -   wherein m is an integer of from 1 to 10; R₁₄, R₁₅, R₁₆, R₁₇,            and R₁₈ are each independently selected from H, C₁₋₆ alkyl,            C₁₋₆ haloalkyl, and halo.

In yet another aspect, the present disclosure provides, inter alia, acomposition, including:

at least one polyunsaturated long-chain alkenone derivative of Formula(V):

wherein R₁₉ is a polar head group, and

R₂₀ is a C₃₀₋₄₅ alkenyl having at least one trans double carbon-carbonbond, or R₂₀ is a C₃₀₋₄₅ alkyl.

DESCRIPTION OF THE DRAWINGS

The foregoing aspects and many of the attendant advantages of thisdisclosure will become more readily appreciated as the same becomebetter understood by reference to the following detailed description,when taken in conjunction with the accompanying drawings.

FIG. 1A shows the structure of an embodiment of an alkenone produced byIsochyrsis sp. As used herein, the nomenclature for alkenonescorresponds to the total number of carbons:number of double bonds.

FIG. 1B shows the structure of an embodiment of a fatty acid,specifically linoleic acid. The alkenone nomenclature corresponds to thetotal number of carbons:number of double bonds.

FIG. 1C is a photograph of alkenones extracted from algae, showing awhite waxy solid.

FIG. 2 shows the structure of an embodiment of saturated fatty acids,specifically stearic acid from animal fat; and the structure of anembodiment of unsaturated fatty acid, specifically oleic acid from oliveoil. Fatty acid nomenclature is given as number of carbons:number ofcis-double bonds. Without wishing to be bound by theory, it is believedthat the incorporation of a cis-alkene into a fatty acid structureprovides a compound that is a less ideal emollient by increasingfluidity and decreasing (oxidative) stability.

FIG. 3 is a scheme of a representative synthesis of a cetyl ester,myristyl myristate, made by reversible condensation of myristic acidwith tetradecanol. Tetradecanol is itself a reduction product ofmyristic acid, and can be made under harsh reaction conditions (e.g.,lithium aluminum hydride, LiAlH₄).

FIG. 4 is a comparison of 37:3 methyl alkenone to the correspondinghydrogenated alkanone and to cetyl palmitate, a fatty emollient. Whilethe molecular formulas and melting points are similar, alkenones andalkanones are not prone to hydrolysis because they lack an esterlinkage.

FIG. 5 is a comparison of a fatty-acid based emulsifier, glycerylmonostearate (GMS), and an alkenone-derived emulsifier glycerylmonoalkenone (“GMA”). The properties of an emulsifier are dependent onthe so-called hydrophilic-lipophilic balance (HLB), i.e., the relativesizes of the hydrophilic and lipophilic portions of the molecule. TheHLB value of monoacylated alkenone glyceryl emulsifiers such as GMA isdifferent than GMS and other fatty acid emulsifiers and providessuperior performance. Stearic acid, used to make GMS, is an animalproduct.

FIG. 6 is an illustration of an embodiment of an alkenone-based cholinephosphate encapsulation system to improve active agent (*) delivery. Thelonger hydrocarbon chain length of alkenones compared to fatty acids(see, e.g., FIGS. 1A and 1B) that have traditionally been used forencapsulation methods can provide unique secondary and tertiarystructures (e.g., liposomes and micelles with elongated hydrophobicregions).

FIG. 7 is an embodiment of an extraction sequence of alkenones fromalgae.

FIG. 8 is a schematic representation of exemplary pathways forconverting alkenones to surface active agents where: R^(A) is H ormethyl and R^(C) is an alkyl group (C_(n)H_(2n+1), e.g., CH₃). X is NHand Y is O. When derived from an alkenone of the present disclosure,R^(B) can be a C₃₂₋₃₇ hydrocarbon chain containing one or more transcarbon-carbon double bonds. For example, R^(B is C) ₃₃ for an alkenonehaving 37 total carbons and R^(A) is H; R^(B) is C₃₄ for an alkenonehaving 38 total carbons and R^(A) is H; and R^(B) is C₃₃ for an alkenonehaving 38 total carbons and R^(A) is methyl. As described in U.S.application Ser. No. 14/599,460 (“the '460 Application”), this R^(B)hydrocarbon chain can be modified to R^(B)≥C₅ alkene (generallycontaining one alkene) or C₅ alkyl.

FIG. 9 shows exemplary IR spectra of alkenones and alkenols, where theloss of the C═O stretch at 1711 cm⁻¹ and emergence of a new O—H stretchoccurs upon reduction of the alkenones to alkenols.

DETAILED DESCRIPTION

The present disclosure describes the use of alkenones andalkenone-derived compounds in eco-friendly personal care products. Thedisclosure also provides methods for the manipulation of algal extractsto provide various combinations of alkenones along with other naturallyoccurring compounds such as oils (e.g., fatty acids and derivatives) andpigments (e.g., carotenoids and chlorophylls). In other aspects,alkenones and/or synthetic alkenone derivatives are used to providepersonal care compositions with desirable properties ranging from mildskin cleansers to cosmetics.

Referring to FIG. 1A, alkenones of the present disclosure havestructures that are characterized by very long hydrocarbon chains (e.g.,36 to 40 carbons; approximately twice as long as typical fatty acids),giving these compounds high melting points (˜70° C.) and making themwhite waxy solids at room temperature. They contain trans-doublecarbon-carbon bonds—as opposed to less stable cis-configured methyleneinterrupted double bonds present in fatty acids (FIG. 1B)—and are amethyl or ethyl ketone.

The alkenones of the present disclosure can be biologically synthesizedby the marine microalgae Isochrysis. Isochrysis provides manyadvantages. For example, Isochrysis is one of only a few species ofalgae with a history of industrial production and is one of only aselect number of algae that biosynthesize a unique suite of lipids knownas polyunsaturated long-chain alkenones (PULCA). Long-chain unsaturatedmethyl and ethyl ketones (alkenones) are part of a group of unusualcompounds including related alkenes and alkenoates collectively referredto as PULCAs. In addition to Isochrysis, alkenones can be biosynthesizedby other haptophyte microalgae, including the ocean coccolithophoridEmiliania huxleyi and the closely related species Gephyrocapsa oceanica.Often these neutral lipids are more abundant than triacylglycerols,especially in the stationary-phase of growth curves. It is believed thatPULCAs reside in cytoplasmic lipid bodies for energy storage. See, e.g.,Eltgroth, M. L., et al., “Production and cellular localization oflong-chain neutral lipids in the haptophyte algae Isochrysis galbana andEmiliania huxleyi,” J. Phycol. 2005, 41, 1000-1009.

Definitions

At various places in the present specification, substituents ofcompounds of the disclosure are disclosed in groups or in ranges. It isspecifically intended that the disclosure include each and everyindividual subcombination of the members of such groups and ranges. Forexample, the term “C₁₋₆ alkyl” is specifically intended to individuallydisclose methyl, ethyl, C₃ alkyl, C₄ alkyl, C₅ alkyl, and C₆ alkyl.

It is further appreciated that certain features of the disclosure, whichare, for clarity, described in the context of separate embodiments, canalso be provided in combination in a single embodiment.

Conversely, various features of the disclosure which are, for brevity,described in the context of a single embodiment, can also be providedseparately or in any suitable subcombination.

As used herein, the term “substituted” or “substitution” refers to thereplacing of a hydrogen atom with a substituent other than H. Forexample, an “N-substituted piperidin-4-yl” refers to replacement of theH atom from the NH of the piperidinyl with a non-hydrogen substituentsuch as, for example, alkyl.

As used herein, the nomenclature for alkenones corresponds to the totalnumber of carbons:number of double bonds. A methyl or ethyl substituenton the alkenone is indicated as Me or Et, respectively.

As used herein, the term “alkyl” refers to a saturated hydrocarbon groupwhich is straight-chained (e.g., linear) or branched. Example alkylgroups include methyl (Me), ethyl (Et), propyl (e.g., n-propyl andisopropyl), butyl (e.g., n-butyl, isobutyl, t-butyl), pentyl (e.g.,n-pentyl, isopentyl, neopentyl), and the like. An alkyl group cancontain from 1 to about 50, from 1 to about 45, from 1 to about 40, from1 to about 30, from 1 to about 24, from 2 to about 24, from 1 to about20, from 2 to about 20, from 1 to about 10, from 1 to about 8, from 1 toabout 6, from 1 to about 4, or from 1 to about 3 carbon atoms.

As used herein, the term “aryl” refers to monocyclic or polycyclic(e.g., having 2, 3, or 4 fused rings) aromatic hydrocarbons such as, forexample, phenyl, naphthyl, anthracenyl, phenanthrenyl, indanyl, andindenyl. In some embodiments, aryl groups have from 6 to about 20 carbonatoms.

As used herein, “arylene” refers to a linking aryl group.

As used herein, the term “halo” or “halogen” includes fluoro, chloro,bromo, and iodo.

As used herein, the term “alkylene” refers to a linking alkyl group.

As used herein, “alkenyl” refers to an alkyl group having one or moredouble carbon-carbon bonds. The double bond can be trans or cis, wherewhen the two alkyl groups are on the same side of the C═C, the doublebond is referred to as cis; and when the alkyl groups are oriented inopposing directions, the double is referred to as trans. The alkenylgroup can be linear or branched. Example alkenyl groups include ethenyl,propenyl, and the like. An alkenyl group can contain from 2 to about 50,from 2 to about 45, from 2 to about 40, from 2 to about 35, from 2 toabout 30, from 2 to about 24, from 2 to about 20, from 2 to about 10,from 2 to about 8, from 2 to about 6, or from 2 to about 4 carbon atoms.

As used herein, “alkenylene” refers to a linking alkenyl group.

As used herein, “alkynyl” refers to an alkyl group having one or moretriple carbon-carbon bonds. The alkynyl group can be linear or branched.Example alkynyl groups include ethynyl, propynyl, and the like. Analkynyl group can contain from 2 to about 50, from 2 to about 45, from 2to about 40, from 2 to about 35, from 2 to about 30, from 2 to about 24,from 2 to about 20, from 2 to about 10, from 2 to about 8, from 2 toabout 6, or from 2 to about 4 carbon atoms.

As used herein, “alkynylene” refers to a linking alkynyl group.

As used herein, “alkoxy” refers to an —O-alkyl group. Example alkoxygroups include methoxy, ethoxy, propoxy (e.g., n-propoxy andisopropoxy), t-butoxy, and the like.

As used herein, “haloalkyl” refers to an alkyl group having one or morehalogen substituents. Example haloalkyl groups include CF₃, C₂F₅, CHF₂,CCl₃, CHCl₂, C₂Cl₅, and the like.

As used herein, “haloalkenyl” refers to an alkenyl group having one ormore halogen substituents.

As used herein, “haloalkynyl” refers to an alkynyl group having one ormore halogen substituents.

As used herein, “haloalkoxy” refers to an —O—(haloalkyl) group.

As used herein, “cycloalkyl” refers to non-aromatic carbocyclesincluding cyclized alkyl, alkenyl, and alkynyl groups. Cycloalkyl groupscan include mono- or polycyclic (e.g., having 2, 3 or 4 fused rings)ring systems, including spirocycles. In some embodiments, cycloalkylgroups can have from 3 to about 20 carbon atoms, 3 to about 14 carbonatoms, 3 to about 10 carbon atoms, or 3 to 7 carbon atoms. Cycloalkylgroups can further have 0, 1, 2, or 3 double bonds and/or 0, 1, or 2triple bonds. Also included in the definition of cycloalkyl are moietiesthat have one or more aromatic rings fused (i.e., having a bond incommon with) to the cycloalkyl ring, for example, benzo derivatives ofpentane, pentene, hexane, and the like. A cycloalkyl group having one ormore fused aromatic rings can be attached though either the aromatic ornon-aromatic portion. One or more ring-forming carbon atoms of acycloalkyl group can be oxidized, for example, having an oxo or sulfidosubstituent. Example cycloalkyl groups include cyclopropyl, cyclobutyl,cyclopentyl, cyclohexyl, cycloheptyl, cyclopentenyl, cyclohexenyl,cyclohexadienyl, cycloheptatrienyl, norbomyl, norpinyl, norcamyl,adamantyl, and the like.

As used herein, “cycloalkylene” refers to a linking cycloalkyl group.

As used herein, “heteroalkyl” refers to an alkyl group having at leastone heteroatom such as sulfur, oxygen, or nitrogen.

As used herein, “heteroalkylene” refers to a linking heteroalkyl group.

As used herein, a “heteroaryl” refers to an aromatic heterocycle havingat least one heteroatom ring member such as sulfur, oxygen, or nitrogen.Heteroaryl groups include monocyclic and polycyclic (e.g., having 2, 3or 4 fused rings) systems. Any ring-forming N atom in a heteroaryl groupcan also be oxidized to form an N-oxo moiety. Examples of heteroarylgroups include without limitation, pyridyl, N-oxopyridyl, pyrimidinyl,pyrazinyl, pyridazinyl, triazinyl, furyl, quinolyl, isoquinolyl,thienyl, imidazolyl, thiazolyl, indolyl, pyrryl, oxazolyl, benzofuryl,benzothienyl, benzthiazolyl, isoxazolyl, pyrazolyl, triazolyl,tetrazolyl, indazolyl, 1,2,4-thiadiazolyl, isothiazolyl, benzothienyl,purinyl, carbazolyl, benzimidazolyl, indolinyl, and the like. In someembodiments, the heteroaryl group has from 1 to about 20 carbon atoms,and in further embodiments from about 3 to about 20 carbon atoms. Insome embodiments, the heteroaryl group contains 3 to about 14, 3 toabout 7, or 5 to 6 ring-forming atoms. In some embodiments, theheteroaryl group has 1 to about 4, 1 to about 3, or 1 to 2 heteroatoms.

As used herein, “heteroarylene” refers to a linking heteroaryl group.

As used herein, “amino” refers to NH₂.

As used herein, “alkylamino” refers to an amino group substituted by analkyl group.

As used herein, “dialkylamino” refers to an amino group substituted bytwo alkyl groups.

As used herein, the term “fatty acid” refers to a molecule having acarboxylic acid with a long aliphatic chain, which is either saturatedor unsaturated.

As used herein, the term “fatty acid ester” refers to a long aliphaticchain (saturated or unsaturated) having a —C(O)O— moiety at an end ofthe chain.

As used herein, the term “fatty acid amide” refers to a long aliphaticchain (saturated or unsaturated) having a —C(O)NR— moiety at an end ofthe chain.

As used herein, the term “constitutional unit” of a polymer refers to anatom or group of atoms in a polymer, comprising a part of the chaintogether with its pendant atoms or groups of atoms, if any. Theconstitutional unit can refer to a repeat unit. The constitutional unitcan also refer to an end group on a polymer chain. For example, theconstitutional unit of polyethylene glycol can be —CH₂CH₂O—corresponding to a repeat unit, or —CH₂CH₂OH corresponding to an endgroup.

As used herein, the term “repeat unit” corresponds to the smallestconstitutional unit, the repetition of which constitutes a regularmacromolecule (or oligomer molecule or block).

As used herein, the term “end group” refers to a constitutional unitwith only one attachment to a polymer chain, located at the end of apolymer. For example, the end group can be derived from a monomer unitat the end of the polymer, once the monomer unit has been polymerized.As another example, the end group can be a part of a chain transferagent or initiating agent that was used to synthesize the polymer.

As used herein, the term “terminus” of a polymer refers to aconstitutional unit of the polymer that is positioned at the end of apolymer backbone.

As used herein, the term “biodegradable” refers to a process thatdegrades a material via hydrolysis and/or a catalytic degradationprocess, such as enzyme-mediated hydrolysis and/or oxidation. Forexample, polymer side chains can be cleaved from the polymer backbonevia either hydrolysis or a catalytic process (e.g., enzyme-mediatedhydrolysis and/or oxidation).

As used herein, “biocompatible” refers to a property of a moleculecharacterized by it, or its in vivo degradation products, being not, orat least minimally and/or reparably, injurious to living tissue; and/ornot, or at least minimally and controllably, causing an immunologicalreaction in living tissue. As used herein, “physiologically acceptable”is interchangeable with biocompatible.

As used herein, the term “hydrophobic” refers to a moiety that is notattracted to water with significant apolar surface area at physiologicalpH and/or salt conditions. This phase separation can be observed via acombination of dynamic light scattering and aqueous NMR measurements.Hydrophobic constitutional units tend to be non-polar in aqueousconditions. Examples of hydrophobic moieties include alkyl groups, arylgroups, etc.

As used herein, the term “hydrophilic” refers to a moiety that isattracted to and tends to be dissolved by water. The hydrophilic moietyis miscible with an aqueous phase. Hydrophilic constitutional units canbe polar and/or ionizable in aqueous conditions. Hydrophilicconstitutional units can be ionizable under aqueous conditions and/orcontain polar functional groups such as amides, hydroxyl groups, orethylene glycol residues. Examples of hydrophilic moieties includecarboxylic acid groups, amino groups, hydroxyl groups, etc.

As used herein, the term “cationic” refers to a moiety that ispositively charged, or ionizable to a positively charged moiety underphysiological conditions. Examples of cationic moieties include, forexample, amino, ammonium, pyridinium, imino, sulfonium, quaternaryphosphonium groups, etc.

As used herein, the term “anionic” refers to a functional group that isnegatively charged, or ionizable to a negatively charged moiety underphysiological conditions. Examples of anionic groups includecarboxylate, sulfate, sulfonate, phosphate, etc.

Unless otherwise defined, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art. Although methods and materials similar or equivalent to thosedescribed herein can be used in the practice or testing of the presentdisclosure, suitable methods and materials are described below. Allpublications, patent applications, patents, and other referencesmentioned herein are incorporated by reference in their entirety. Incase of conflict, the present specification, including definitions, willcontrol. In addition, the materials, methods, and examples areillustrative only and not intended to be limiting.

Personal Care Compositions

As discussed above, in one aspect, the present disclosure features apersonal care composition including one or more alkenones oralkenone-derived compounds, such as a compound of Formula (I):

wherein

R₁ is methyl or ethyl; and

R₂ is a C₃₀₋₄₅ alkenyl having at least one trans double carbon-carbonbond, or R₂ is a C₃₀₋₄₅ alkyl;

provided that the compound of Formula (I) is not

In another aspect, the personal care composition includes a compound ofFormula (I):

wherein

R₁ is methyl or ethyl; and

R₂ is a C₃₀₋₄₅ alkenyl having at least one trans double carbon-carbonbond.

In yet another aspect, the personal care composition includes a compoundof Formula (I):

wherein

R₁ is methyl or ethyl; and

R₂ is a C₃₂₋₄₅ alkyl;

provided that the compound of Formula (I) is not

In a further aspect, the personal care composition includes a compoundof Formula (I):

wherein

R₁ is methyl or ethyl; and

R₂ is a C₃₃₋₄₅ alkyl;

provided that the compound of Formula (I) is not

In yet another aspect, the present disclosure features a personal carecomposition, including at least one compound of Formula (II), Formula(III), or Formula (IV):

wherein

R₃ is selected from —OH, —O(CH₂CH₂)_(n)OSO₃—, and —O(CH₂)(CHOH)(CHOH),

-   -   wherein n is an integer of from 1 to 200, and

R₂ is a C₃₀₋₄₅ alkenyl having at least one trans double carbon-carbonbond, or R₂ is a C₃₀₋₄₅ alkyl;

wherein

R₁ is methyl or ethyl;

R₂ is a C₃₀₋₄₅ alkenyl having at least one trans double carbon-carbonbond, or R₂ is a C₃₀₋₄₅ alkyl;

R₄, R₅, and R₆ are each independently selected from H, C₁₋₆ alkyl, C₁₋₆haloalkyl, and halo; and

R₇ is selected from H and —CO₂—;

wherein

R₁ is methyl or ethyl;

R₂ is a C₃₀₋₄₅ alkenyl having at least one trans double carbon-carbonbond, or R₂ is a C₃₀₋₄₅ alkyl;

R₈ is selected from —SO₃—, PO₂—OR₉, and —CONHR₁₀,

-   -   wherein R₉ is —CH₂CH₂N⁺R₁₁R₁₂R₁₃, wherein R₁₁, R₁₂, and R₁₃ are        each independently selected from H, C₁₋₆ alkyl, C₁₋₆ haloalkyl,        and halo, and    -   R₁₀ is (CH₂)_(m)SO₃—, (CH₂)_(m)N⁺R₁₄R₁₅CH₂CO₂—,        (CH₂)_(m)N⁺R₁₆R₁₇R₁₈,        -   wherein m is an integer of from 1 to 10; R₁₄, R₁₅, R₁₆, R₁₇,            and R₁₈ are each independently selected from H, C₁₋₆ alkyl,            C₁₋₆ haloalkyl, and halo.

In yet another aspect, the present disclosure features a personal carecomposition, including at least one compound of Formula (II), Formula(III), or Formula (IV):

wherein

R₃ is selected from —OH, —O(CH₂CH₂)_(n)OSO₃—, and —O(CH₂)(CHOH)(CHOH),

-   -   wherein n is an integer of from 1 to 200, and

R₂ is a C₃₀₋₄₅ alkenyl having at least one trans double carbon-carbonbond, or R₂ is a C₃₆₋₄₅ alkyl;

wherein

R₁ is methyl or ethyl;

R₂ is a C₃₀₋₄₅ alkenyl having at least one trans double carbon-carbonbond, or R₂ is a C₃₆₋₄₅ alkyl;

R₄, R₅, and R₆ are each independently selected from H, C₁₋₆ alkyl, C₁₋₆haloalkyl, and halo; and

R₇ is selected from H and —CO₂—;

wherein

R₁ is methyl or ethyl;

R₂ is a C₃₀₋₄₅ alkenyl having at least one trans double carbon-carbonbond, or R₂ is a C₃₆₋₄₅ alkyl;

R₈ is selected from —SO₃—, —PO₂—OR₉, and —CONHR₁₀,

-   -   wherein R₉ is —CH₂CH₂N⁺R₁₁R₁₂R₁₃, wherein R₁₁, R₁₂, and R₁₃ are        each independently selected from H, C₁₋₆ alkyl, C₁₋₆ haloalkyl,        and halo, and    -   R₁₀ is —(CH₂)_(m)SO₃—, —(CH₂)_(m)N⁺R₁₄R₁₅CH₂CO₂—,        —(CH₂)_(m)N⁺R₁₆R₁₇R₁₈,        -   wherein m is an integer of from 1 to 10; R₁₄, R₁₅, R₁₆, R₁₇,            and R₁₈ are each independently selected from H, C₁₋₆ alkyl,            C₁₋₆ haloalkyl, and halo.

In yet another aspect, the present disclosure features a compositionincluding at least one compound of Formula (V):

wherein R₁₉ is a polar head group, and

R₂₀ is a C₃₀₋₄₅ alkenyl having at least one trans double carbon-carbonbond, or R₂₀ is a C₃₀₋₄₅ alkyl.

Aspects of the compositions above can have one or more of the followingfeatures.

In some embodiments, R₂ is an alkenyl having at least 34 carbons and atleast one trans double carbon-carbon bond.

In some embodiments, R₂ is an alkenyl having at least 35 carbons and atleast one trans double carbon-carbon bond.

In some embodiments, R₂ is a C₃₄₋₄₅ alkenyl having at least one transdouble carbon-carbon bond.

In some embodiments, R₂ is a C₃₅₋₄₅ alkenyl having at least one transdouble carbon-carbon bond.

In some embodiments, R₂ is a C₃₆₋₄₅ alkenyl having at least one transdouble carbon-carbon bond.

In some embodiments, R₂ is a C₃₄₋₄₀ alkenyl having at least one transdouble carbon-carbon bond.

In some embodiments, R₂ is a C₃₅₋₄₀ alkenyl having at least one transdouble carbon-carbon bond.

In some embodiments, R₂ is a C₃₆₋₄₀ alkenyl having at least one transdouble carbon-carbon bond.

In some embodiments, R₂ has 2 to 4 trans double carbon-carbon bonds.

In some embodiments, R₂ has 2 trans double carbon-carbon bonds.

In some embodiments, R₂ has 3 trans double carbon-carbon bonds.

In some embodiments, R₂ has 4 trans double carbon-carbon bonds.

In some embodiments, R₂ is a C₃₃₋₄₀ alkyl.

In some embodiments, R₂ is a C₃₄₋₄₀ alkyl.

In some embodiments, R₂ is a C₃₅₋₄₀ alkyl.

In some embodiments, R₂ is a C₃₆₋₄₀ alkyl.

In some embodiments, R₂ is C₃₂ alkyl.

In some embodiments, R₂ is C₃₃ alkyl.

In some embodiments, R₂ is C₃₄ alkyl.

In some embodiments, R₂ is C₃₅ alkyl.

In some embodiments, R₂ is C₃₆ alkyl.

In some embodiments, R₂ is C₃₇ alkyl.

In some embodiments, R₂ is C₃₈ alkyl.

In some embodiments, R₂ is C₃₉ alkyl.

In some embodiments, R₂ is C₄₀ alkyl.

It is understood that the definitions above for R₁ and R₂ can becombined in any manner.

In some embodiments, R₂₀ is an alkenyl having at least 34 carbons and atleast one trans double carbon-carbon bond.

In some embodiments, R₂₀ is an alkenyl having at least 35 carbons and atleast one trans double carbon-carbon bond.

In some embodiments, R₂₀ is a C₃₅₋₄₅ alkenyl having at least one transdouble carbon-carbon bond.

In some embodiments, R₂₀ is a C₃₆₋₄₅ alkenyl having at least one transdouble carbon-carbon bond.

In some embodiments, R₂₀ is a C₃₅₋₄₀ alkenyl having at least one transdouble carbon-carbon bond.

In some embodiments, R₂₀ is a C₃₆₋₄₀ alkenyl having at least one transdouble carbon-carbon bond.

In some embodiments, R₂₀ has 2 to 4 trans double carbon-carbon bonds.

In some embodiments, R₂₀ has 2 trans double carbon-carbon bonds.

In some embodiments, R₂₀ has 3 trans double carbon-carbon bonds.

In some embodiments, R₂₀ has 4 trans double carbon-carbon bonds.

In some embodiments, R₂₀ is a C₃₃₋₄₀ alkyl.

In some embodiments, R₂₀ is a C₃₄₋₄₀ alkyl.

In some embodiments, R₂₀ is a C₃₅₋₄₀ alkyl.

In some embodiments, R₂₀ is a C₃₆₋₄₀ alkyl.

In some embodiments, R₂₀ is C₃₂ alkyl.

In some embodiments, R₂₀ is C₃₃ alkyl.

In some embodiments, R₂₀ is C₃₄ alkyl.

In some embodiments, R₂₀ is C₃₅ alkyl.

In some embodiments, R₂₀ is C₃₆ alkyl.

In some embodiments, R₂₀ is C₃₇ alkyl.

In some embodiments, R₂₀ is C₃₈ alkyl.

In some embodiments, R₂₀ is C₃₉ alkyl.

In some embodiments, R₂₀ is C₄₀ alkyl.

In some embodiments, the compound of Formula (I) is not one or more ofthe following compounds:

In some embodiments, the compound of Formula (I) is selected from thegroup consisting of:

-   -   wherein R₁ is methyl or ethyl, and R_(2-C34) is C₃₄ alkenyl        having 2 or 3 trans double carbon-carbon bonds:

-   -   wherein R₁ is methyl or ethyl, and R_(2-C35) is C₃₅ alkenyl        having 2 or 3 trans double carbon-carbon bonds;

-   -   wherein R₁ is methyl or ethyl, and R_(2-C36) is C₃₆ alkenyl        having 2 or 3 trans double carbon-carbon bonds;

-   -   wherein R₁ is methyl or ethyl, and R_(2-C37) is C₃₇ alkenyl        having 1, 2, 3, or 4 trans double carbon-carbon bonds;

-   -   wherein R₁ is methyl or ethyl, and R_(2-C38) is C₃₈ alkenyl        having 1, 2, 3, or 4 trans double carbon-carbon bonds; and

-   -   wherein R₁ is methyl or ethyl and R_(2-C39) is C₃₉ alkenyl        having 1, 2, 3, or 4 trans double carbon-carbon bonds.

In some embodiments, R₂ has two or more trans double carbon-carbonbonds, and at least two of the trans double carbon-carbon bonds arespaced from one another by 5 carbon atoms. For example, the compound ofFormula (I) can be one or more of

In some embodiments, the composition includes a majority component(e.g., greater than 50% by weight of the total weight of the compoundsfor formula (I)) including one or more of:

In some embodiments, the composition includes one or more of thefollowing compounds for Formula (I):

In some embodiments, the compound of formula (I) is one or more of

In some embodiments, m is 1 or 2.

In some embodiments, in the compound of Formula (II), (III), or (IV), R₂is independently a C₃₄₋₄₅ alkenyl having at least one trans doublecarbon-carbon bond.

In some embodiments, in the compound of Formula (II), (III), or (IV), R₂is independently a C₃₅₋₄₅ alkenyl having at least one trans doublecarbon-carbon bond.

In some embodiments, in the compound of Formula (II), (III), or (IV), R₂is independently a C₃₆₋₄₅ alkenyl having at least one trans doublecarbon-carbon bond.

In some embodiments, in the compound of Formula (II), (III), or (IV), R₂is independently a C₃₄₋₄₀ alkenyl having at least one trans doublecarbon-carbon bond.

In some embodiments, in the compound of Formula (II), (III), or (IV), R₂is independently a C₃₅₋₄₀ alkenyl having at least one trans doublecarbon-carbon bond.

In some embodiments, in the compound of Formula (II), (III), or (IV), R₂is independently a C₃₆₋₄₀ alkenyl having at least one trans doublecarbon-carbon bond.

In some embodiments, in the compound of Formula (II), (III), or (IV), R₂independently comprises 2 to 4 trans double carbon-carbon bonds.

In some embodiments, in the compound of Formula (II), (III), or (IV), R₂independently comprises 3 trans double carbon-carbon bonds.

In some embodiments, in the compound of Formula (II), (III), or (IV), R₂is independently selected from:

C₃₄ alkenyl having 2 or 3 trans double carbon-carbon bonds;

C₃₅ alkenyl having 2 or 3 trans double carbon-carbon bonds;

C₃₆ alkenyl having 2 or 3 trans double carbon-carbon bonds;

C₃₇ alkenyl having 1, 2, 3, or 4 trans double carbon-carbon bonds;

C₃₈ alkenyl having 1, 2, 3, or 4 trans double carbon-carbon bonds; and

C₃₉ alkenyl having 1, 2, 3, or 4 trans double carbon-carbon bonds.

In some embodiments, in the compound of Formula (II), (III), or (IV), R₂is independently selected from:

R₂ is C₃₄ alkenyl having 2 or 3 trans double carbon-carbon bonds;

R₂ is C₃₅ alkenyl having 2 or 3 trans double carbon-carbon bonds;

R₂ is C₃₆ alkenyl having 2 or 3 trans double carbon-carbon bonds;

R₂ is C₃₇ alkenyl having 1, 2, 3, or 4 trans double carbon-carbon bonds;

R₂ is C₃₈ alkenyl having 1, 2, 3, or 4 trans double carbon-carbon bonds;and

R₂ is C₃₉ alkenyl having 1, 2, 3, or 4 trans double carbon-carbon bonds.

In some embodiments, R₂ has two or more trans double carbon-carbonbonds, and at least two of the trans double carbon-carbon bonds areseparated from one another by 5 carbon atoms. For example, R₂ in thecompounds of Formula (II), Formula (III), or Formula (IV) canindependently selected from

In some embodiments, in the compound of Formula (II), (III), or (IV), R₂is C₃₀₋₄₅ alkyl (e.g., C₃₄₋₄₅ alkyl, C₃₅₋₄₅ alkyl, C₃₆₋₄₅ alkyl, C₃₇₋₄₅alkyl, C₃₈₋₄₅ alkyl, C₃₉₋₄₅ alkyl, C₄₀₋₄₅ alkyl, C₃₄ alkyl, C₃₅ alkyl,C₃₆ alkyl, C₃₇ alkyl, C₃₈ alkyl, C₃₉ alkyl, or C₄₀ alkyl).

In some embodiments, n is an integer of from 1 to 100 (e.g., 1 to 50, 1to 20, 1 to 10, 1 to 5, 5 to 50, 5 to 20, 5 to 10, 10 to 50, or 10 to20).

In some embodiments, R₄, R₅, and R₆ are each independently selected fromH, C₁₋₆ alkyl, and halo.

In some embodiments, R₄, R₅, and R₆ are each independently selected fromH and C₁₋₆ alkyl.

In some embodiments, R₄, R₅, and R₆ are each independently selected fromH and methyl.

In some embodiments, R₄, R₅, and R₆ are each H.

In some embodiments, R₈ is selected from —PO₂—OR₉ and —CONHR₁₀,

-   -   wherein R₉ is —CH₂CH₂N⁺R₁₁R₁₂R₁₃, wherein R₁₁, R₁₂, and R₁₃ are        each independently selected from H, C₁₋₆ alkyl, C₁₋₆ haloalkyl,        and halo, and    -   R₁₀ is —(CH₂)_(m)SO₃—, —(CH₂)_(m)N⁺R₁₄R₁₅CH₂CO₂—,        —(CH₂)_(m)N⁺R₁₆R₁₇R₁₈,        -   wherein m is an integer of from 1 to 10; R₁₄, R₁₅, R₁₆, R₁₇,            and R₁₈ are each independently selected from H, C₁₋₆ alkyl,            C₁₋₆ haloalkyl, and halo.

In some embodiments, R₁₁, R₁₂, and R₁₃ are each independently selectedfrom H, C₁₋₆ alkyl, and halo.

In some embodiments, R₁₁, R₁₂, and R₁₃ are each independently selectedfrom H and C₁₋₆ alkyl.

In some embodiments, R₁₁, R₁₂, and R₁₃ are each independently selectedfrom H and methyl.

In some embodiments, R₁₁, R₁₂, and R₁₃ are each H.

In some embodiments, R₁₄, R₁₅, R₁₆, R₁₇, and R₁₈ are each independentlyselected from H, C₁₋₆ alkyl, and halo.

In some embodiments, R₁₄, R₁₅, R₁₆, R₁₇, and R₁₈ are each independentlyselected from H and C₁₋₆ alkyl.

In some embodiments, R₁₄, R₁₅, R₁₆, R₁₇, and R₁₈ are each independentlyselected from H and methyl.

In some embodiments, R₁₄, R₁₅, R₁₆, R₁₇, and R₁₈ are each H.

In some embodiments, the compound of Formula (I), (II), (III), or (IV)has a melting temperature of 70° C. or less (e.g., 60° C. or less, 50°C. or less, 40° C. or less, or 30° C.).

In some embodiments, the compound of Formula (I), (II), (III), or (IV)is a waxy solid at 25° C. In some embodiments, the compound of Formula(I), (II), (III), or (IV) is a waxy solid at 30° C. (e.g., 40° C., 50°C., 60° C., 70° C., or 80° C.).

In some embodiments, the composition is in the form of a topicalcomposition, such as a skin-care composition, a hair-care composition,and/or a cosmetic composition.

In some embodiments, the compound of Formula (I), (II), (III), or (IV)functions as an emollient, an abrasive, an occlusive agent, anencapsulating agent, a stabilizing agent, a binding agent, a thickeningagent, a surfactant, an antimicrobial agent, or any combination thereof.

In some embodiments, the compound of Formula (I), (II), (III), or (IV)is present from 1 to 50% w/w (e.g., from 1 to 40%, from 1 to 30%, orfrom 1 to 20%) of the total composition.

In some embodiments, the compound of Formula (I), (II), (III), or (IV)is isolated from algae such as Isochrysis, Emiliania huxleyi, and/orGephyrocapsa oceanica, or derived (i.e., through chemical synthesis)from the algae-isolated compound of Formula (I), (II), (III), or (IV).

In some embodiments, the polar head group R₁₉ is an alcohol, an ester,an acid, a carboxylate, a sulfonate, a phosphonate, and/or ammonium.

In some embodiments, the composition does not include anypetroleum-based waxes or oils, plant-based fats, animal-based fats,and/or any combination thereof. For example, the alkenone or thealkenone derivative in the composition can be solely derived from analgae such as Isochrysis, Emiliania huxleyi, and/or Gephyrocapsaoceanica.

In some embodiments, the composition further includes an oil, a fattyacid, or both. In some embodiments, the composition further includes asurfactant such as a C₄₋₂₈ fatty acid carboxylate, a C₄₋₂₈ alkylsulfate, a C₄₋₂₈ alkyl betaine, and/or an alkenone-derived surfactant.

In some embodiments, the compositions of the present disclosure furtherinclude a synthetic agent selected from synthetic solubilizing agents,synthetic emulsifying agents, synthetic humectants, syntheticemollients, synthetic occlusive agents, synthetic surfactants, syntheticpreservatives, synthetic binding agents, synthetic thickeners, syntheticsolvents, synthetic fragrances, and any combination thereof.

In some embodiments, the compositions of the present disclosure furtherinclude a naturally occurring agent selected from natural emollients,natural occlusive agents, natural emulsifying agents, naturalanti-oxidants, natural colorants, natural fragrances, and anycombination thereof.

In some embodiments, the composition further includes one or more mono-,di-, or triglycerides and/or one or more alcohols. In some embodiments,the composition is an encapsulant.

In some embodiments, the one or more compounds of the present disclosureare purified (e.g., whitened by, for example, decolorizing withactivated charcoal) prior to incorporation into the composition.

In some embodiments, the compositions of the present disclosure do notinclude any petroleum-based waxes or oils, plant-based fats,animal-based fats, and/or any combination thereof. For example, thealkenone or the alkenone derivative in the compositions of the presentdisclosure can be solely derived from an algae such as Isochrysis,Emiliania huxleyi, and/or Gephyrocapsa oceanica.

In some embodiments, the compositions of the present disclosure furtherinclude an oil (e.g., an acylglycerol), a fatty acid, or both. In someembodiments, the composition further includes a surfactant such as aC₄₋₂₈ fatty acid carboxylate, a C₄₋₂₈ alkyl sulfate, a C₄₋₂₈ alkylbetaine, and/or an alkenone-derived surfactant.

In some embodiments, the compounds of Formula (I), Formula (II), Formula(III) and/or Formula (IV) are present from 1 to 50% w/w (e.g., from 1 to40%, from 1 to 30%, or from 1 to 20%) of the total alkenone oralkenone-derivative content in the composition.

As will be explained in greater detail below, in certain embodiments,the compositions of the present disclosure are emollients. Thecompositions of the present disclosure can further include a surfactant(a fatty acid carboxylate, a sulfate, a betaine, and/or analkenone-derived surfactant). For example, a given composition can be askin cleanser.

Compositions Containing Alkenones and/or Alkenone-Derived Compounds

This compositions of the present disclosure use unique but abundantalgal lipids to address growing concerns about the use of petroleum notonly for fuels, but other products such as those in personal care andrelated industries to feed a burgeoning market for “green” non-petroleumproducts. Topical compositions including the compounds of the presentdisclosure include emulsions that can be generally divided into threecategories, based on viscosity: low viscosity lotions, medium viscositycreams, and high viscosity ointments. Examples of products includeabrasive soaps, with alkenones and/or alkenone-derived compounds servingas natural exfoliating agents. Alkenones and their derivatives in thesecompositions can serve as emollients, occlusive agents, encapsulatingagents, stabilizing agents, binding agents, thickening agents,surfactants, and antimicrobials. Other roles for alkenones includeproviding products with desired textural, tactile, and aestheticqualities, all of which have historically been achieved with petroleum.

The personal care composition can be a skin care, anti-perspirant,deodorant, cosmetic, or hair care product. The personal care compositioncan be used as, for example, a moisturizer, conditioner, anti-agingcompound, skin lightener, sunscreen, sunless tanner, shave preparation,lipstick, foundation, mascara, after-shave, and combinations thereof. Incertain embodiments, the composition is applied to the face, neck,hands, arms, and other typically exposed areas of the body.

The personal care composition can be in a wide variety of forms.Non-limiting examples include simple solutions (e.g., water or oilbased), dispersions, and emulsions. The personal care composition can besubstantially anhydrous (i.e., the composition comprises no more thanabout 1%, 0.5%, or, 0% water). The personal care compositions can befluid or solid (gels, sticks, flowable solids, amorphous materials). Incertain embodiments, the personal care composition is in the form of anemulsion. Emulsion can be generally classified as having a continuousaqueous phase (e.g., oil-in-water and water-in-oil-in-water) or acontinuous oil phase (e.g., water-in-oil and oil-in-water-in-oil).

The compositions of the present disclosure can include a variety ofother components in addition to the alkenone and/or alkenone-derivedcompounds. For example, the compositions can include solubilizingagents, emulsifying agents, humectants, emollients, occlusive agents,surfactants, preservatives, binding agents, thickeners, solvents,antioxidants, colorants, and/or fragrances; each of which can benaturally occurring or man-made (i.e., synthetic).

Synthetic Components

Examples of synthetic solubilizing agents include alkyl and acylglucosides, polyethylene glycols, and polysaccharides.

Examples of synthetic emulsifying agents include fatty alcohol (C8-C20)(poly)glucosides, (poly)glyceryl fatty alcohols, polyethylene fattyalcohols, fatty acid (poly)glucosides, (poly)glyceryl fatty acids, andpolyhydroxy fatty acids.

Examples of synthetic humectants include propylene glycol, butyleneglycol, and pentylene glycol.

Examples of synthetic emollients include fatty alcohol esters(e.g.cetearyl ethylhexanoate, isoamyl cocoate, isoamyl laurate),polyglyceryl fatty acids (e.g., polyglyceryl-6-stearate), andpolyglyceryl sebecates.

Examples of synthetic occlusive agents include siloxanes, sodiumhyaluronate, and hydrolyzed polyglutamic acids.

Examples of synthetic surfactants include sodium lauryl sarcosinate, andfatty alcohol glucosides (e.g., caprylyl-capryl glucoside).

Examples of synthetic preservatives include phenoxyethanol, benzylalcohol, glycerol ethers, and alkylparabens.

Examples of synthetic binding agents include EDTA and sodium phytate.

Examples of synthetic thickeners include polyacrylates (carbomer),propylene glycol, and siloxanes.

Examples of synthetic solvents include ethylene glycol and propyleneglycol,

Examples of synthetic fragrances include aldehydes and esters.

Natural Components

Examples of natural emollients include lanolin, allantoin, shea butter,and trehalose.

Examples of natural occlusive agents include glycerin, citric acid, andmineral oil.

Examples of natural emulsifying agents include triglycerides andlecithin.

Examples of natural anti-oxidants include tocopherol.

Examples of natural colorants include clays.

Examples of natural fragrances include botanical extracts.

Carriers, Emulsifiers

In some embodiments, the personal care composition can include acarrier. Carriers can be selected for various stability, aesthetics,and/or compatibility with other materials present in the personal carecomposition.

Suitable carriers include water and/or water soluble solvents. Thepersonal care composition can include from about 1% to about 95% byweight of water and/or water-equivalent solvent. The composition caninclude from about 1%, 3%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%,50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, or 90% to about 90%, 85%, 80%,75%, 70%, 65%, 60%, 55%, 50%, 45%, 40%, 35%, 30%, 25%, 20%, 15%, 10%, or5% water and/or a water-equivalent solvent. “Water-equivalent solvent”refers to a compound which has a similar ability as water to solubilizea material. Suitable water-equivalent solvents include monohydricalcohols, dihydric alcohols, polyhydric alcohols, glycerol, glycols,polyalkylene glycols such as polyethylene glycol, and mixtures thereof.Examples of suitable solvents include lower aliphatic alcohols such asethanol, propanol, butanol, isopropanol; diols such as 1,2-propanediol,1,3-propanediol, butanediol, pentanediol, hexanediol, heptanediol,decanediol; glycerin; water, and mixtures thereof. In certainembodiments, the personal care includes comprises water, diols,glycerin, and combinations thereof.

Suitable carriers also include oils. The personal care composition caninclude from about 1% to about 95% by weight of one or more oils. Thecomposition can include from about 1%, 3%, 5%, 10%, 15%, 20%, 25%, 30%,35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, or 90% to about90%, 85%, 80%, 75%, 70%, 65%, 60%, 55%, 50%, 45%, 40%, 35%, 30%, 25%,20%, 15%, 10%, or 5% of one or more oils. Oils can be used tosolubilize, disperse, or carry materials that are not suitable for wateror water-equivalent solvents. Suitable oils include silicones,hydrocarbons, esters, fatty amides, ethers, and mixtures thereof. Oilscan be fluid at room temperature. However, certain personal care productforms (i.e., solid or semi-solid stick) can include non-fluid oils. Theoils can be volatile or nonvolatile. “Non-volatile” means a materialthat exhibits a vapor pressure of no more than about 0.2 mm Hg at 25° C.at one atmosphere and/or a material that has a boiling point at oneatmosphere of at least about 300° C. “Volatile” means that the materialexhibits a vapor pressure of at least about 0.2 mm of mercury at 20° C.Volatile oils can be used to provide a lighter feel when a heavy, greasyfilm is undesirable.

Suitable oils include volatile oils. In certain embodiments, thevolatile oils can have a viscosity ranging from about 0.5 to about 5centistokes 25° C. Volatile oils can be used to promote more rapiddrying of the skin care composition after it is applied to skin.Nonvolatile oils are also suitable for use in the composition.Nonvolatile oils can be used for emolliency and protective properties.Nonvolatile oils can have a viscosity ranging from about 5 to about800,000 cst (or greater) or from about 20 to about 200,000 cst.

Suitable silicone oils include polysiloxanes. Polysiloxanes can have aviscosity of from about 0.5 to about 1,000,000 centistokes at 25° C.Commercially available polysiloxanes include the polydimethylsiloxanes,which are also known as dimethicones, examples of which include theDM-Fluid series from Shin-Etsu, the Vicasil® series sold by MomentivePerformance Materials Inc., and the Dow Corning® 200 series sold by DowCorning Corporation. Specific examples of suitable polydimethylsiloxanesinclude Dow Corning® 200 fluids (also sold as Xiameter® PMX-200 SiliconeFluids) having viscosities of 0.65, 1.5, 50, 100, 350, 10,000, 12,500,100,000, and 300,000 centistokes.

Suitable hydrocarbon oils include straight or branched chain alkanes andalkenes. The chain length can be selected based on desired functionalcharacteristics such as volatility. Suitable hydrocarbon oils can havebetween 5-20 carbon atoms or, alternately, between 8-16 carbon atoms.Suitable hydrocarbons include pentane, hexane, heptane, decane,dodecane, tetradecane, tridecane, and C₈₋₂₀ isoparaffins. Suitablehydrocarbons include isooctane, isododecane, isohexadecane, isoeicosaneby Permethyl Corporation under the tradename Permethyl®. Suitablehydrocarbon oils can have greater than about 20 carbon atoms. Examplesof such hydrocarbon oils include C₂₄₋₂₈ olefins, C₃₀₋₄₅ olefins, C₂₀₋₄₀isoparaffins, hydrogenated polyisobutene, polyisobutene, polydecene,hydrogenated polydecene, mineral oil, pentahydrosqualene, squalene,squalane, and mixtures thereof.

Other suitable oils include esters. Suitable esters typically contain atleast 10 carbon atoms. These esters include esters with hydrocarbylchains derived from fatty acids or alcohols (e.g., mono-esters,polyhydric alcohol esters, and di- and tri-carboxylic acid esters). Thehydrocarbyl radicals of the esters hereof can include or have covalentlybonded thereto other compatible functionalities, such as amides andalkoxy moieties (e.g., ethoxy or ether linkages, etc.). Exemplary estersinclude, but are not limited to, isopropyl isostearate, hexyl laurate,isohexyl laurate, isohexyl palmitate, isopropyl palmitate, decyl oleate,isodecyl oleate, hexadecyl stearate, decyl stearate, isopropylisostearate, dihexyldecyl adipate, lauryl lactate, myristyl lactate,cetyl lactate, oleyl stearate, oleyl oleate, oleyl myristate, laurylacetate, cetyl propionate, and oleyl adipate. Other suitable esters arefurther described in the Personal Care Product Council's InternationalCosmetic Ingredient Dictionary and Handbook, Thirteenth Edition, 2010,under the functional category of “Esters.”

Other esters suitable for use in the personal care composition includemono-carboxylic acid esters such as C₁₂₋₁₅ alkyl benzoate.

Other esters suitable for use in the personal care composition includedi- and tri-alkyl and alkenyl esters of carboxylic acids, such as estersof C₄ to C₈ dicarboxylic acids (e.g., C₁ to C₂₂ esters, preferably C₁ toC₆, of succinic acid, glutaric acid, and adipic acid). Specificnon-limiting examples of di- and tri-alkyl and alkenyl esters ofcarboxylic acids include isocetyl stearoyl stearate, diisopropyladipate, dibutyl adipate, and tristearyl citrate.

Other esters suitable for use in the personal care composition includethose known as polyhydric alcohol esters. Such polyhydric alcohol estersinclude alkylene glycol esters, such as ethylene glycol mono anddi-fatty acid esters, diethylene glycol mono- and di-fatty acid esters,polyethylene glycol mono- and di-fatty acid esters, propylene glycolmono- and di-fatty acid esters, polypropylene glycol monooleate,polypropylene glycol 2000 monostearate, ethoxylated propylene glycolmonostearate, glyceryl mono- and di-fatty acid esters, polyglycerolpoly-fatty acid esters, ethoxylated glyceryl monostearate, 1,3-butyleneglycol monostearate, 1,3-butylene glycol distearate, polyoxyethylenepolyol fatty acid ester, sorbitan fatty acid esters, andpolyoxy-ethylene sorbitan fatty acid esters.

Still other esters suitable for use in the personal care compositioninclude glycerides, including, but not limited to, mono-, di-, andtri-glycerides. For example, the glycerides can be mono-, di-, andtri-esters of glycerol and long chain carboxylic acids, such as C₁₀ toC₂₂ carboxylic acids. A variety of these types of materials can beobtained from vegetable and animal fats and oils, such as castor oil,safflower oil, cottonseed oil, corn oil, olive oil, cod liver oil,almond oil, avocado oil, palm oil, sesame oil, sweet almond oil, apricotkernel oil, camelina sativa oil, rapeseed oil, tamanu seed oil, linseedoil, coconut oil, lanolin oil, soybean oil, and the like. Synthetic oilsinclude, but are not limited to, triolein and tristearin glyceryldilaurate. Other glyceryl esters of fatty acids include fatty acidmono-, di-, and triglycerides which are natural fats or oils that havebeen modified such as glyceryl stearate, diglyceryl diisostearate,polyglyceryl-3 isostearate, polyglyceryl-4 isostearate, polyglyceryl-6ricinoleate, glyceryl dioleate, glyceryl diisostearate, glyceryltetraisostearate, glyceryl trioctanoate, diglyceryl distearate, glyceryllinoleate, glyceryl myristate, glyceryl isostearate, PEG castor oils,PEG glyceryl oleates, PEG glyceryl stearates, PEG glyceryl tallowates,and the like.

Other suitable oils include fatty amides. Fatty amides include compoundshaving an amide functional group while being liquid at 25° C. andinsoluble in water, such as N-acetyl-N-butylaminopropionate, isopropylN-lauroylsarcosinate, and N,N,-diethyltoluamide. Other suitable fattyamides are disclosed in U.S. Pat. No. 6,872,401.

Other suitable oils include ethers. Suitable ethers include saturatedand unsaturated fatty ethers of a polyhydric alcohol, and alkoxylatedderivatives thereof. Exemplary ethers include C₄₋₂₀ alkyl ethers ofpolypropylene glycols, and di-C₈₋₃₀ alkyl ethers. Suitable examples ofthese materials include PPG-14 butyl ether, PPG-15 stearyl ether,dioctyl ether, dodecyl octyl ether, and mixtures thereof.

Emulsifiers

The personal care compositions can include an emulsifier. An emulsifieris particularly suitable when the composition is in the form of anemulsion or if immiscible materials are being combined. The skin carecomposition can include from about 0.05%, 0.1%, 0.2%, 0.3%, 0.5%, or 1%to about 20%, 10%, 5%, 3%, 2%, or 1% emulsifier. Emulsifiers can benonionic, anionic or cationic. Non-limiting examples of emulsifiers aredescribed in McCutcheon's, Emulsifiers and Detergents, 2010 Annual Ed.,published by M. C. Publishing Co. Other suitable emulsifiers are furtherdescribed in the Personal Care Product Council's International CosmeticIngredient Dictionary and Handbook, Thirteenth Edition, 2006, under thefunctional category of “Surfactants—Emulsifying Agents.”

Suitable emulsifying ethers and esters include ethers of polyglycols andof fatty alcohols—including saturated or unsaturated C₁₂₋₃₀ alcohols(e.g., oleyl alcohol, cetyl alcohol, stearyl alcohol or behenyl alcohol)and polyglycols comprising n number of oxyalkylene groups wherein n isan integer from 1 to 200 or, alternately, from 2 to 30 (e.g., 1 to 20oxyethylene groups). Examples of emulsifying ethers and esters includecompounds with the INCI names of steareth-n, beheneth-n or oleth-n. Insome embodiments, examples include compounds having the INCI namessteareth-8, steareth-10, steareth-16, steareth-20, ceteth-10, laureth-4,laureth-3, trideceth-6, ceteareth-5, oleth-10, and beneth-10.

Emulsifiers can include esters of polyglycols and of fattyacids—including saturated or unsaturated C₁₂₋₃₀ fatty acids (e.g., oleicacid, cetylic acid, stearic acid) and polyglycols comprising n number ofoxyalkylene groups wherein n is an integer from 1 to 200 or alternately,1 to 50 (e.g., 1 to 20 oxyethylene groups). Examples include compoundswith the INCI name PEG-n stearate or PEG-n oleate). In some embodiments,examples include polyethylene glycol-8 monostearate, polyethyleneglycol-10, or polyethylene glycol-12 distearate.

Emulsifiers can include ethers of polyglycols and of fatty alcoholswhich are glycosylated—including C₁₂₋₃₀ alcohols having from 1 to 10glycosyl groups and polyglycols comprising n number of oxyalkylenegroups wherein n is an integer from 1 to 200 (e.g., 1 to 20 oxyethylenegroups). A suitable example includes polyoxyethylenated (20 OE) methylglucose distearate.

Examples of emulsifiers include esters of polyglycols and of fatty acidswhich are glycosylated—including C₁₂₋₃₀ fatty acids having from 1 to 10glycosyl groups and polyglycols comprising n number of oxyalkylenegroups wherein n is an integer from 1 to 200 (e.g., 1 to 20 oxyethylenegroups).

Examples of emulsifiers include ethers of C₁₂₋₃₀ alcohols and ofglycerol or of polyglycerol—A suitable example includes polyglyceryl-3cetyl ether, such as Chimexane NL from Chimex.

Examples of emulsifiers include esters of C₁₂₋₃₀ fatty acids and ofglycerol or of polyglycerol—including esters comprising from 1 to 10glycerol groups. Examples include hexa-glyceryl monosterate, diglyceryldistearate, tetraglyceryl tristearate, decaglycerol decastearate,diglyceryl monostearate, hexaglyceryl tristearate, decaglycerolpentastearate, the ester of glycerol and of palmitic and stearic acids,and glyceryl mono- and dibehenate.

Examples of emulsifiers include ethers of oxyalkylene-modified C₁₂₋₃₀alcohols and of glycerol or polyglycerol.

Examples of emulsifiers include ethers of C₁₂₋₃₀ fatty alcoholscomprising and of sucrose or glucose—Suitable examples include compoundswith the INCI names of C₁₂₋₁₈ alkylglucoside, C₁₂₋₂₀ alkylglucoside(e.g., Montanov L from Seppic), cetearyl glucoside (e.g., a mixture withcetearyl alcohol under the reference Montanov 68 from Seppic), myristylglucoside (e.g., a mixture with myristyl alcohol under the referenceMontanov 14 from Seppic) or cetearyl glucoside (e.g., Tegocare CG 90from Evonik Goldschmidt),

Examples of emulsifiers include esters of sucrose and of C₁₂₋₃₀ fattyacids, such as sucrose distearate or sucrose tristearate, sucrosecocoate, sucrose dilaurate, sucrose distearate, sucrose hexaerucate,sucrose hexapalmitate, sucrose laurate, sucrose mortierellate, sucrosemyristate, sucrose oleate, sucrose palmitate, sucrose pentaerucate,sucrose polybehenate, sucrose polycottonseedate, sucrose polylaurate,sucrose polylinoleate, sucrose polyoleate, sucrose polypalmate, sucrosepolysoyate, sucrose polystearate, sucrose ricinoleate, sucrose stearate,sucrose tetraisostearate, and sucrose trilaurate. A suitable exampleincludes the mixture of esters (mono- and polyesters) of stearic acidand of sucrose sold as Crodesta F1 10 by Croda.

Examples of emulsifiers include esters of pentaerythritol and of C₁₂₋₃₀fatty acids, such as pentaerythritol tetrastearate.

Examples of emulsifiers include esters of sorbitol and/or of sorbitanand of C₁₂₋₃₀ fatty acids, such as sorbitan monostearate, sorbitantristearate, or sorbitan laurate, such as Span 20 from Uniqema,

Examples of emulsifiers include ethers of sorbitol and/or of sorbitanand of alkoxylated sorbitan—Suitable examples include sorbeth-8 beeswaxor sorbeth-20 beeswax from Nikko Chemical.

Examples of emulsifiers include esters of C₁₂₋₃₀ fatty acids and ofalkoxylated ethers of sorbitol and/or of Suitable examples includepolysorbate-60, polysorbate-61, sorbeth-3 isostearate,polyoxyethylenated 4 OE sorbitan monostearate, and polyoxyethylenated 20OE sorbitan tristearate.

Structuring Agent

The personal care composition can include a structuring agent toincrease viscosity, thicken, solidify, or provide solid or crystallinestructure to the personal care composition. Examples of aqueous or waterstructuring agents include polymeric agents, natural or synthetic gums,polysaccharides, and the like. In one embodiment, the composition caninclude from about 0.0001%, 0.001%, 0.01%, 0.05%, 0.1%, 0.5%, 1%, 2%,3%, or 5% to about 25%, 20%, 10%, 7%, 5%, 4%, or 2%, by weight of thecomposition, of one or more structuring agents.

Polysaccharides and gums can be used as aqueous phase thickening agents.Classes of polymeric structuring agents include but are not limited tocarboxylic acid polymers (e.g., carbomers), polyacrylamide polymers,sulfonated polymers, high molecular weight polyalkylglycols orpolyglycerins, copolymers thereof, hydrophobically modified derivativesthereof (e.g., oil structuring agents, silicone elastomers, siliconegums, silicone waxes), and mixtures thereof.

Other structuring agents are natural or synthetic montmorilloniteminerals such as hectorite, bentonite, and quaternized derivativesthereof, which are obtained by reacting the minerals with a quaternaryammonium compound (e.g., stearalkonium bentonite and stearalkoniumhectorite); and silicas, silicates, silica silylate, and alkali metal oralkaline earth metal derivatives thereof.

Optional Personal Care Ingredients

The personal care compositions can include one or more optionalcomponents to provide an efficacious and/or consumer desirable product.For example, the composition can include sugar amines, vitamins, oilcontrol agents, phytosterols, hexamidine compounds, tightening agents,anti-wrinkle actives, anti-atrophy actives, flavonoids, N-acyl aminoacid compounds, retinoids, peptides, particulate materials, UV actives,photostabilizers, anti-cellulite agents, desquamation actives, anti-acneactives, anti-oxidants, radical scavengers, conditioning agents,botanical extracts, preservatives, and/or detersive surfactants, andcombinations thereof.

Examples of sugar amines include glucosamine, N-acetyl glucosamine,mannosamine, N-acetyl mannosamine, galactosamine, N-acetylgalactosamine, their isomers (e.g., stereoisomers), and their salts(e.g., HCl salt). In some embodiments, the sugar amine is glucosamine,such as D-glucosamine and N-acetyl glucosamine. In certain embodiments,the sugar amine is N-acetyl-D-glucosamine.

Examples of vitamins include: vitamin B compounds (including B1compounds, B2 compounds, B3 compound, B5 compounds, such as panthenol or“pro-B5”, pantothenic acid, pantothenyl; B6 compounds, such aspyroxidine, pyridoxal, pyridoxamine; carnitine, thiamine, riboflavin);vitamin A compounds, and all natural and/or synthetic analogs of vitaminA, including retinoids, retinol, retinyl acetate, retinyl palmitate,retinoic acid, retinaldehyde, retinyl propionate, carotenoids(pro-vitamin A), and other compounds which possess the biologicalactivity of vitamin A; vitamin D compounds; vitamin K compounds; vitaminE compounds, or tocopherol, including tocopherol sorbate, tocopherolacetate, other esters of tocopherol and tocopheryl compounds; vitamin Ccompounds, including ascorbate, ascorbyl esters of fatty acids, andascorbic acid derivatives, for example, ascorbyl phosphates such asmagnesium ascorbyl phosphate and sodium ascorbyl phosphate, ascorbylglucoside, and ascorbyl sorbate; and vitamin F compounds, such assaturated and/or unsaturated fatty acids.

Examples of suitable oil control agents include salicylic acid,dehydroacetic acid, benzoyl peroxide, vitamin B3 compounds, theirisomers, esters, salts and derivatives, and mixtures thereof. Examplesof oil absorbing materials include starch, calcium silicate,polyethylene, nylon, boran nitride, mica, clays such as bentonite,montmorillonite and kaolin, zeolite, cyclodextrins, fumed silica,synthetic clays such as polymer powders including natural, synthetic,and semisynthetic cellulose, fluorocarbon resins, polypropylene,modified starches of cellulose acetate, particulate cross-linkedhydrophobic acrylate or methacrylate copolymers and mixtures thereof. Inone embodiment, the personal care composition can include from about0.001%, 0.01%, 0.05%, 0.1%, 0.5%, or 1% to about 25%, 20%, 10%, 7%, 5%,or 3% by weight of the composition, of one or more oil control agents.

Examples of phytosterols include β-sitosterol, campesterol,brassicasterol, Δ5-avenasterol, lupenol, α-spinasterol, stigmasterol,their derivatives, analogs, and combinations thereof. In one embodiment,the composition can include from about 0.0001%, 0.001%, 0.01%, 0.05%,0.1%, 0.5%, or 1% to about 25%, 20%, 10%, 7%, 5%, or 3%, by weight ofthe composition, of one or more phytosterol.

In some embodiments, the personal care composition includes a tighteningagent. A tightening agent is a compound capable of having a tighteningeffect on keratinous tissues and, typically, on skin. Examples oftightening agents can include plant or animal proteins and theirhydrolysates such as maize, rye, wheat, buckwheat, sesame, spelt, pea,bean, lentil, soybean and lupin; polysaccharides of natural originincluding (i) polyholosides, for example, in the form of starch derivedespecially from rice, maize, potato, cassaya, peas, wheat, oats, etc.,or in the form of carrageenans, alginates, agars, gellans, cellulosepolymers and pectins, advantageously as an aqueous dispersion of gelmicroparticles, and (ii) lattices composed of shellac resin, gumsandarac, dammars, elemis, copals, cellulose compounds, and mixturesthereof; mixed silicates including phyllosilicates (e.g., laponites);colloidal particles of inorganic fillers such as silica/aluminacolloidal particles such as those sold under then tradename LUDOX® byW.R. Grace & Co.; synthetic polymers such as polyurethane lattices oracrylic/silicone lattices (e.g., propylthio(polymethyl acrylate)),propylthio(polymethyl methacrylate) and propylthio(polymethacrylic acid)grafted polydimethylsiloxane, propyl-thio(polyisobutyl methacrylate) andpropylthio(poly-methacrylic acid) grafted polydimethylsiloxane(available under the tradenames VS 80, VS 70 and L021 from 3M); andmixtures thereof. The personal care composition can include from about0.0001%, 0.001%, 0.01%, 0.05%, 0.1%, 0.5%, or 1% to about 30%, 25%, 20%,10%, 7%, 5%, or 3% by weight of the composition, of one or moretightening agent.

Exemplary anti-wrinkle/anti-atrophy actives include dialkanoylhydroxyproline compounds, hydroxy acids (e.g., glycolic acid, lacticacid, lactobionic acid), keto acids (e.g., pyruvic acid), phytic acid,lysophosphatidic acid, stilbenes, cinnamates, resveratrol, kinetin,zeatin, dimethylaminoethanol, peptides from natural sources (e.g., soypeptides), and salts of sugar acids (e.g., Mn gluconate, Zn gluconate).In one embodiment, the composition can include from about 0.0001%,0.001%, 0.01%, 0.05%, 0.1%, 0.5%, or 1% to about 30%, 25%, 20%, 10%, 7%,5%, or 3% by weight of the composition, of one or moreanti-wrinkle/anti-atrophy compounds.

The compositions of the present invention can comprise a flavonoidcompound, such as flavones, isoflavones, coumarins, chromones,dicoumarols, chromanones, chromanols, isomers (e.g., cis/trans isomers)thereof, and mixtures thereof. In one embodiment, the compositionincludes from about 0.0001%, 0.001%, 0.01%, 0.05%, 0.1%, 0.5%, or 1% toabout 30%, 25%, 20%, 10%, 7%, 5%, or 3%, by weight of the composition,of one or more flavonoid compounds.

Examples of N-acyl amino acid compound include N-acyl Phenylalanine,N-acyl Tyrosine, their isomers, their salts, and derivatives thereof,such as N-undecylenoyl-L-phenylalanine. In one embodiment, thecomposition can include from about 0.0001%, 0.001%, 0.01%, 0.05%, 0.1%,0.5%, or 1% to about 30%, 25%, 20%, 10%, 7%, 5%, or 3%, by weight of thecomposition, of one or more N-acyl amino acids.

In one embodiment, the composition can include from about 0.0001%,0.001%, 0.01%, 0.05%, 0.1%, 0.5%, or 1% to about 30%, 25%, 20%, 10%, 7%,5%, or 3%, by weight of the composition, of one or more retinoids. Asused herein, “retinoid” includes natural and/or synthetic analogs ofVitamin A or retinol-like compounds which possess the biologicalactivity of Vitamin A in the skin as well as the geometric isomers andstereoisomers of these compounds. The retinoid can include retinol,retinol esters (e.g., C₂-C₂₂ alkyl esters of retinol, including retinylpalmitate, retinyl acetate, retinyl propionate), retinal, and/orretinoic acid (including all-trans retinoic acid and/or 13-cis-retinoicacid), or mixtures thereof. Other retinoids include tocopheryl-retinoate[tocopherol ester of retinoic acid (trans- or cis-), adapalene(6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthoic acid}, and tazarotene(ethyl 6-[2-(4,4-dimethylthiochroman-6-yl)-ethynyl]nicotinate).

Examples of peptides can include, but are not limited to, di-, tri-,tetra-, penta-, and hexa-peptides and derivatives thereof. In oneembodiment, the compositions include from about 1×10⁻⁷% to about 20%,from about 1×10⁻⁶% to about 10%, or from about 1×10⁻⁵% to about 5%, byweight of a peptide. In one embodiment, the composition includes fromabout 0.0001%, 0.001%, 0.01%, 0.05%, 0.1%, 0.5%, or 1% to about 25%,20%, 10%, 7%, 5%, 3%, by weight of the composition, of one or morepeptides. As used herein, “peptide” refers to peptides containing ten orfewer amino acids and their derivatives, isomers, and complexes withother species such as metal ions (e.g., copper, zinc, manganese,magnesium, and the like). Peptide refers to both naturally occurring andsynthesized peptides. Examples of peptides include the dipeptidecarnosine (beta-ala-his), the tripeptide gly-his-lys, the tripeptidehis-gly-gly, the tripeptide gly-gly-his, the tripeptide gly-his-gly, thetetrapeptide gly-gln-pro-arg, the pentapeptide lys-thr-thr-lys-ser,lipophilic derivatives of peptides, and metal complexes of theaforementioned (e.g., copper complex of the tripeptide his-gly-gly (alsoknown as Iamin)). Other suitable peptides include Peptide CK(arg-lys-arg); Peptide CK+ (ac-arg-lys-arg-NH2); and Peptide E,arg-ser-arg-lys.

Examples of particulate materials useful in the present disclosureinclude colored and uncolored pigments, interference pigments, inorganicpowders, organic powders, composite powders, optical brightenerparticles, and combinations thereof. In one embodiment, the compositionincludes from about 0.0001%, 0.001%, 0.01%, 0.05%, 0.1%, 0.5%, 1%, or 2%to about 50%, 25%, 20%, 10%, 7%, 5%, or 3% by weight of the composition,of particulate(s).

Examples of inorganic pigments include iron oxides, ferric ammoniumferrocyanide, manganese violet, ultramarine blue, and Chrome oxide.Organic pigments can include natural colorants and synthetic monomericand polymeric colorants. An example is phthalocyanine blue and greenpigment. Also useful are lakes, primary FD&C or D&C lakes and blendsthereof. Also useful are encapsulated soluble or insoluble dyes andother colorants. Inorganic white or uncolored pigments useful in thepresent invention, for example TiO₂, ZnO, or ZrO₂, are commerciallyavailable from a number of sources. One example of a suitableparticulate material contains the material available from U.S. Cosmetics(TRONOX TiO₂ series, SAT-T CR837, a rutile TiO₂). Suitable pigmentsinclude charged dispersions of titanium dioxide, as are disclosed inU.S. Pat. No. 5,997,887.

The compositions can contain a UV active, such as sunscreen agents andphysical sunblocks. Suitable UV actives can be organic or inorganic.Suitable UV actives are listed in the functional category of “SunscreenAgents” in the Personal Care Product Council's International CosmeticIngredient Dictionary and Handbook, Thirteenth Edition, 2010. Examplesof UV actives include 2-ethylhexyl-p-methoxycinnamate,4-tert-butyl-4′-methoxy dibenzoylmethane,2-hydroxy-4-methoxybenzo-phenone, 2-phenylbenzimidazole-5-sulfonic acid,octocrylene, zinc oxide, titanium dioxide, and mixtures thereof.

Examples of photostabilizer include ethylhexyl methoxycrylene, or2-ethylhexyl 2-cyano-3-(4-methoxyphenyl)-3-phenylpropenoate;diethylhexyl 2,6-naphthalate, ethyl-alpha-cyano-3,5-dimethoxy-4-hydroxycinnamate, ethyl-alpha-acetyl-3,5-dimethoxy-4-hydroxy cinnamate,iso-propyl-alpha-acetyl-3,5-dimethoxy-4-hydroxy cinnamate,iso-amyl-alpha-acetyl-3,5-dimethoxy-4-hydroxy cinnamate,2-ethylhexyl-alpha-acetyl-3,5-dimethoxy-4-hydroxy cinnamate,diethyl-3,5-dimethoxy-4-hydroxy benzylidene malonate,di-(2-ethylhexyl)-3,5-dimethoxy-4-hydroxy benzylidene malonate,diisoamyl-3,5-dimethoxy-4-hydroxy benzylidene malonate,didodecyl-3,5-dimethoxy-4-hydroxy benzylidene malonate,dipalmitoyl-3,5-dimethoxy-4-hydroxy benzylidene malonate, anddi-isopropyl-3,5-dimethoxy-4-hydroxy benzylidene malonate. In oneembodiment, the composition can include from about 0.0001%, 0.001%,0.01%, 0.05%, 0.1%, 0.5%, or 1% to about 30%, 25%, 20%, 10%, 7%, or 5%,by weight of the composition, of one or more suitable photostabilizer.

Examples of anti-cellulite agents include caffeine, theophylline,theobromine, aminophylline, chloroethyltheophylline, dyphylline,etamiphyllin, proxyphylline; extracts of tea, coffee, guarana, mate,cola (Cola nitida); extracts of climbing ivy (Hedera helix), arnica(Arnica montana L), rosemary (Rosmarinus officinalis N), of marigold(Calendula officinalis), sage (Salvia officinalis L), ginseng (Panaxginseng), St. John's wort (Hypericum perforatum), of butcher's broom(Ruscus aculeatus L), meadowsweet (Filipendula ulmaria L), orthosiphon(Orthosiphon stamincus benth), birch (Betula alba), cecropia and argantree; Ginkgo biloba, horsetail, escin, cangzhu, Chrysanthellum indicum,Dioscorea plants rich in diosgenin or pure diosgenin or hecogenin andcompounds thereof, Ballota, Guioa, Davallia, Terminalia, Barringtonia,Trema, Antirobia, bitter orange (Citrus aurantium); and an extract ofcocoa bean shells (Theobroma cacao) such as sold under the nameCaobromine® by Solabia. In one embodiment, the personal care compositioncan include from about 0.0001%, 0.001%, 0.01%, 0.05%, 0.1%, 0.5%, or 1%to about 30%, 25%, 20%, 10%, 7%, 5%, or 3%, by weight of thecomposition, of one or more anti-cellulite agents.

In one embodiment, the composition can include from about 0.0001%,0.001%, 0.01%, 0.05%, 0.1%, 0.5%, or 1% to about 30%, 25%, 20%, 10%, 7%,5%, or 3%, by weight of the composition, of one or more desquamationactives. Examples of desquamation actives include beta-hydroxy acidssuch as salicylic acid and its derivatives (including5-(noctanoyl)salicylic acid also known as capryloyl salicylic acid) andalpha-hydroxy acids such as glycolic acid, citric acid, lactic acid,tartaric acid, malic acid or mandelic acid;8-hexadecene-1,16-dicarboxylic acid or 9-octadecanedioic acid; urea;gentisic acid; oligofucoses; cinnamic acid; Saphora Japonica extract;and resveratrol.

Examples of anti-acne actives include resorcinol, sulfur, salicylicacid, retinoids such as retinoic acid and its derivatives,sulfur-containing amino acids and their derivatives and salts (e.g.,N-acetyl derivatives such as N-acetyl-L-cysteine), and lipoic acid;benzoyl peroxide, octopirox, tetracycline, 2,4,4′ trichloro-2′-hydroxydiphenyl ether, 3,4,4′-trichloroaniline, azelaic acid and itsderivatives, phenoxyethanol, phenoxypropanol, phenoxyisopropanol, ethylacetate, clindamycin and meclocycline. In one embodiment, thecomposition includes from about 0.0001%, 0.001%, 0.01%, 0.05%, 0.1%,0.5%, or 1% to about 30%, 25%, 20%, 10%, 7%, 5%, or 3%, by weight of thecomposition, of one or more anti-acne compounds.

In one embodiment, the composition can include from about 0.0001%,0.001%, 0.01%, 0.05%, 0.1%, 0.5%, or 1% to about 30%, 25%, 20%, 10%, 7%,5%, or 3%, by weight of the composition, of one or moreanti-oxidant/radical scavengers. Examples of anti-oxidants includebutylated hydroxytoluene (BHT) and butylated hydroxyanisole (BHA);ascorbic acid (vitamin C), tocopherol (vitamin E), tocopherol sorbate,tocopherol acetate, other esters of tocopherol,6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (commerciallyavailable under the tradename Trolox®), amines (e.g.,N,N-diethylhydroxylamine, amino-guanidine), nordihydroguaiaretic acid,bioflavonoids, amino acids, silymarin, sorbic acids and its salts,lipoic acid, olive extracts, green tea extracts, white tea extracts,black tea extracts, polyphenols such as proanthocyanidin from pine bark,carotenoids, curcumin compounds such as tetrahydrocurcumin, OCTA(L-2-oxo-4-thiazolidine carboxylic acid), glutathione, and grapeskin/seed extracts can be used. Suitable anti-oxidants/radicalscavengers can be selected from esters of tocopherol such as tocopherolacetate.

The personal care compositions of the present invention can contain asafe and effective amount of a conditioning agent selected from, forexample, humectants, moisturizers, occlusives, and emollients which canbe applied to keratinous tissue. In one embodiment, the composition caninclude from about 0.0001%, 0.001%, 0.01%, 0.05%, 0.1%, 0.5%, or 1% toabout 50%, 25%, 20%, 10%, 7%, or 5%, by weight of the composition, ofone or more conditioning agents.

Humectants are one group of conditioning agents. Examples of humectantsinclude polyhydric alcohols, water soluble alkoxylated nonionicpolymers, and mixtures thereof. Examples of polyhydric alcohols includeglycerin, sorbitol, propylene glycol, butylene glycol, pentylene glycol,hexylene glycol, ethoxylated glucose, 1,2-hexane diol, hexanetriol,dipropylene glycol, erythritol, trehalose, diglycerin, xylitol,maltitol, maltose, glucose, fructose, sodium chondroitin sulfate, sodiumhyaluronate, hyaluronic acid, sodium adenosine phosphate, sodiumlactate, pyrrolidone carbonate, glucosamine, cyclodextrin, and mixturesthereof. Examples of water soluble alkoxylated nonionic polymers includepolyethylene glycols and polypropylene glycols having a molecular weightof up to about 1000 such as those with CTFA names PEG-200, PEG-400,PEG-600, PEG-1000, and mixtures thereof.

Examples of conditioning agents include guanidine, urea, glycolic acid,glycolate salts (e.g. ammonium and quaternary alkyl ammonium), salicylicacid, lactic acid, lactate salts (e.g., ammonium and quaternary alkylammonium), aloe vera in any of its variety of forms (e.g., aloe veragel), polyethylene glycols, sugars (e.g., melibiose), cellulose,dextrin, starches, sugar and starch derivatives (e.g., alkoxylatedglucose, fucose), lactamide monoethanolamine, acetamidemonoethanolamine, panthenol, allantoin, amylose, hyaluronic acid, sodiumhyaluronate, betaglucan, glycogen, alguronic acid, galactoarabinan andmixtures thereof; extracts that contain polysaccharides such as TriMoistKMF (Mibelle AG Biochemistry), Fucogel® and Glycofilm® (Solabia Group),Aquaxyl™ (Seppic), Pheohydrane P (Barnet Products Corporation),Aesthigel (Barnet Products Corporation), Pentacare HP (Pentapharm), andHyalurosmooth (Laboratoires Serobiologiques); C₁-C₃₀ monoesters andpolyesters of sugars and related materials.

The personal care composition can include botanical extracts. In oneembodiment, the composition includes from about 0.0001%, 0.0005% 0.001%,0.01%, 0.05%, 0.1%, 0.5%, or 1% to about 30%, 25%, 20%, 10%, 7%, 5%, or3%, by weight of the composition, of one or more botanical extracts.Examples of botanical extracts include extracts from plants (herbs,roots, flowers, fruits, seeds) such as flowers, fruits, vegetables, andso on, including yeast ferment extract, Padina Pavonica extract, thermusthermophilis ferment extract, camelina sativa seed oil, boswelliaserrata extract, olive extract, bodopsis Thaliana extract, AcaciaDealbata extract, Acer Saccharinum (sugar maple), acidopholus, acorns,aesculus, Alicaligenes polysaccharides, agaricus, agave, agrimonia,algae, aloe, citrus, brassica, cinnamon, orange, apple, blueberry,cranberry, peach, pear, lemon, lime, pea, seaweed, caffeine, green tea,chamomile, willowbark, mulberry, poppy, and the like. Further specificexamples include, but are not limited to, Glycyrrhiza Glabra, SalixNigra, Macrocycstis Pyrifera, Pyrus Malus, Saxifraga Sarmentosa, VitisVinifera, Morus Nigra, Scutellaria Baicalensis, Anthemis Nobilis, SalviaSclarea, Rosmarinus Officianalis, Citrus Medica Limonum, Ginkgo BilobaPanax Ginseng, Siegesbeckia Orientalis, Fructus Mume, AscophyllumNodosum, Bifida Ferment lysate, Glycine Soja extract, Beta Vulgaris,Haberlea Rhodopensis, Polygonum Cuspidatum, Citrus Aurantium Dulcis,Vitis Vinifera, Selaginella Tamariscina, Humulus Lupulus, CitrusReticulata Peel, Punica Granatum, Asparagopsis, Curcuma Longa,Menyanthes Trifoliata, Helianthus Annuus, Hordeum Vulgare, CucumisSativus, Evernia Prunastri, Evernia Furfuracea, Laminaria Angustata,Laminaria Cloustoni, Laminaria Digitata, Laminaria Digitata, LaminariaHyperborea, Laminaria Japonica, Laminaria Longissima, LaminariaOchotensis, Laminaria Ochroleuca, Laminaria Saccharina, and mixturesthereof. Other suitable actives are listed in the functional category of“Biological Products” in the Personal Care Product Council'sInternational Cosmetic Ingredient Dictionary and Handbook, ThirteenthEdition, 2010.

In one embodiment, the composition includes from about 0.0001%, 0.001%,0.01%, 0.05%, 0.1%, 0.5%, or 1% to about 10%, 7%, 5%, 2%, or 1%, byweight of the composition, of one or more preservatives. Examples ofpreservatives include benzoic acid, benzyl alcohol, benzylhemiformal,benzylparaben, 5-bromo-5-nitro-1,3-dioxane,2-bromo-2-nitropropane-1,3-diol, butyl paraben, phenoxyethanol, methylparaben, propyl paraben, diazolidinyl urea, sodium benzoate, calciumbenzoate, calcium propionate, caprylyl glycol, biguanide derivatives,phenoxyethanol, captan, chlorhexidine diacetate, chlorhexidinedigluconate, chlorhexidine dihydrochloride, chloroacetamide,chlorobutanol, p-chloro-m-cresol, chlorophene, chlorothymol,chloroxylenol, m-cresol, o-cresol, DEDM hydantoin, DEDM hydantoindilaurate, dehydroacetic acid, diazolidinyl urea, dibromopropamidinediisethionate, DMDM hydantoin, glyceryl caprylate, potassium sorbate,salicylic acid, hexamidine, capryloyl glycine, 1,2 hexanediol,undecylenoyl glycine, ethylhexylglycerin, caprylhydroxamic acid,methylpropanediol, hinokitiol, sodium hinokitiol, phenylethyl alcohol,levulinec acid, p-anisic acid, 2-bromo-2-nitropropane-1,3-diol, sodiumhydroxymethylglycinate, iodopropynyl butylcarbamate,methylchloroisothiazolinone, methylisothiazolinone, piroctone olamine,cinnamon oil, rosemary extract, Biopein® (available form Bio-Botanica),Naticide® (available form Sinerga), and combinations thereof. In oneembodiment, the composition is free of parabens and/or formaldehydes.

Depending upon the form and function, the personal care composition caninclude one or more detersive surfactants. If and when present, thedetersive surfactant component can be included to provide cleaningperformance to the composition. The detersive surfactant component inturn can comprise anionic detersive surfactant, zwitterionic oramphoteric detersive surfactant, or a combination thereof.

The composition can include from about 1%, 2.5%, 5%, 7.5%, 10%, 12.5%,or 15% to about 50%, 40%, 30%, 25%, 20%, or 10%, by weight of thedetersive surfactants in the composition. Examples of anionic detersivesurfactants include ammonium lauryl sulfate, ammonium laureth sulfate,triethylamine lauryl sulfate, triethylamine laureth sulfate,triethanolamine lauryl sulfate, triethanolamine laureth sulfate,monoethanolamine lauryl sulfate, monoethanolamine laureth sulfate,diethanolamine lauryl sulfate, diethanolamine laureth sulfate, lauricmonoglyceride sodium sulfate, sodium lauryl sulfate, sodium laurethsulfate, potassium lauryl sulfate, potassium laureth sulfate, sodiumlauryl sarcosinate, sodium lauroyl sarcosinate, lauryl sarcosine, cocoylsarcosine, ammonium cocoyl sulfate, ammonium lauroyl sulfate, sodiumcocoyl sulfate, sodium lauroyl sulfate, potassium cocoyl sulfate,potassium lauryl sulfate, triethanolamine lauryl sulfate,triethanolamine lauryl sulfate, monoethanolamine cocoyl sulfate,monoethanolamine lauryl sulfate, sodium tridecyl benzene sulfonate,sodium dodecyl benzene sulfonate, sodium cocoyl isethionate andcombinations thereof.

Examples of amphoteric detersive surfactants include cocoamphoacetate,cocoamphodiacetate, lauroamphoacetate, lauroamphodiacetate, and mixturesthereof. Examples of other anionic, zwitterionic, amphoteric or optionaladditional surfactants are described in McCutcheon's, Emulsifiers andDetergents, 2010 Annual Ed., published by M. C. Publishing Co., and U.S.Pat. Nos. 3,929,678, 2,658,072, 2,438,091, and 2,528,378.

Emollient Compositions Including Alkenones or Alkenone-Derived Compounds

Dermatitis is a general term describing inflammation of the skin. It canhave many causes and occurs in many forms, but usually involves an itchyrash and/or swollen, reddened skin. In the U.S., approximately 31.6million people are afflicted with some form of dermatitis. Emollientsare agents used to treat dermatitis, which generally come in the form ofcreams, ointments, or lotions. They help skin feel more comfortable bymaintaining skin moisture and flexibility thereby preventing painfulcracking and other irritations. When used regularly, emollients can beused to treat mild to moderate eczema. See, e.g., “Emollients,” NationalEczema Society, www.eczema.org/emollients.

Even for those not suffering from eczema/atopic dermatitis, variousdaily-use emollient formulations are available to combat general skinirritation. Repeated skin cleansing, while an important component ofoverall well-being and personal health, is very drying to the skin. Inaddition to removing dirt, sebum residues, and microorganisms, cleansingcan also remove or disrupt essential skin oils resulting in dryness andirritation. Post-cleansing emollient-containing creams, lotions, showergels, etc., can restore and maintain skin health.

Aside from being used to treat skin ailments, emollients are also commonto a number of skin-care, hair-care, and cosmetic products to improvesensorial properties both during application and final after-feel. Anemollient's chemical nature and associated physical properties such asspreading attributes, viscosity, and lubricity each contribute to itsperformance in formulation. The structures of algal polyunsaturatedlong-chain alkenones and alkenone derivatives of the present disclosureare uniquely suited to serve as emollients, compared to existingemollients based on waxes and oils from petroleum (e.g., paraffin wax,petroleum jelly, mineral oil, etc.), silicones, or fatty acids, whichcan pose certain environmental and potential toxicity hazards. See,e.g., European Centre for Ecotoxicology and Toxicology of Chemical,Linear Polydimethylsiloxanes (viscosity 10-100,000 centistokes), ECETOCJoint Assessment of Commodity Chemicals No. 26, September 1994.

For fatty-acid emollients, saturated fats like stearic acid from animalfat are superior to unsaturated fats common to most plants (e.g., oleicacid in olive oil, FIG. 2). Saturated fats exhibit preferred physicalproperties such as higher melting points and viscosities, along withenhanced chemical (i.e., oxidative) stabilities. Examples of thestructure and nomenclature of fatty acids are shown in FIG. 2. However,animal-based products have generally fallen out of favor with the trendtoward more sustainable vegetable-based materials, evidenced by thegrowing vegan movement. See, e.g., Cherry, E. “Veganism as a CulturalMovement: A Relational Approach,” Social Movement Stud. 2006, 5,155-170). Referring to FIG. 3, one example of plant-based saturatedfatty acid emollients is cetyl esters. These are made from a combinationof a saturated fatty acid and fatty alcohol with the resulting waxyesters (m.p. ˜40-60° C.) often used to provide desired properties tocreams and lotions such as thickening, fatting, emulsion enhancing andopacifying effects to various personal care products. For example,referring to FIG. 3, myristyl myristate is made by condensing myristicacid, the primary component of nutmeg oil, with tetradecanol. Thesynthesis of fatty alcohols like tetradecanol is however non-trivial,because reduction of the corresponding fatty acid (e.g., myristic acidfor tetradecanol and palmitic acid for cetyl alcohol) can require hightemperatures/pressures, moisture-free and/or inert gas atmospheres, andcan liberate explosive hydrogen gas. Additionally, the condensationreaction between the fatty acid and alcohol is reversible, making cetylesters potentially hydrolytically unstable.

Accordingly, in one aspect, compositions containing the compounds of thepresent disclosure are creams, ointments, or lotions. In someembodiments, the compositions include an alkenone or alkenone derivativeof the present disclosure, oil (e.g., an acylglycerol), and/or a fattyacid.

By virtue of their long-chain length, alkenones possess the appropriatephysical properties for use as emollients, and can be used in someembodiments without further manipulation (i.e., waxy solids at roomtemperature (m.p.=60-70° C.), with similar properties to cetyl esters).They contain chemically stable trans-double bonds compared to thecis-methylene interrupted alkenes that are responsible for the pooroxidative stability of vegetable-derived fats. Moreover, hydrogenationof the double bonds in the alkenones provides saturated alkenones(“alkanones”) with slightly lower melting points closer to cetyl esters(FIG. 4). Because both alkenones and alkenones do not contain an esterfunctional group but rather a ketone, they are thus not prone tohydrolysis. Alkenones are advantageously biodegraded by aerobic bacteria(see, e.g., Zabeti, N. et al. FEMS Microbiol. Ecol., “Potentialalteration of U^(K) ₃₇ paleothermometer due to selective degradation ofalkenones by marine bacteria isolated from the haptophyte Emilianiahuxleyi,” FEMS Microbiol. Ecol., 2010, 73, 83-94), thereby allowingthese compounds and alkenone derivatives to conform to EPA environmentalsafety standards. See, e.g., Environmental Protection Agency: SaferChoice Standard and Criteria, http://www2epa.gov/saferchoice/standard(accessed Nov. 2, 2015).

Others skin-care compositions including alkenone and alkenonederivatives can improve, restore, and/or maintain skin health, byproviding a moisture barrier as emollients or occlusive agents.Additionally, these compositions can have cosmetic applications such ascreating a desirable waxy sheen in coloring agents (e.g., lipsticks),hair, or other personal products.

In one embodiment, one or more alkenones or alkenone derivatives of thepresent disclosure are present from 1-50% w/w of the total composition.Products made directly from algal oil (approximately 10% w/w alkenones)are typically on the low range of total alkenone content afterformulation. Higher percentage alkenone-containing products outlined inTable 1 below can be achieved by incorporating purified alkenones toperform specific functions in personal care products.

TABLE 1 Alkenone percentage in personal care compositions based on roleof alkenone. Alkenone Role in Composition Preferred Alkenone Content(w/w %) Abrasive  5-15 Wax  5-15 Emollient 10-35 Surfactant 10-35

As an example, an emollient composition can include one or moreacylglycerols, one or more fatty acids; and one or more alkenones. Insome embodiments, the one or more acylglycerols, one or more fattyacids, and the one or more alkenones can each independently be presentin an amount of from 2% (e.g., from 5%, from 8%, or from 10%) to 15%(e.g., to 10%, to 8%, or to 5%) by weight in the emollient composition.

As another example, an alkenone-containing emollient composition cancontain one or more alkenones, one or more oils (e.g., mono-, di-, andtriglycerides), one or more alcohols (e.g., glycerin or fatty alcohols),and water. In some embodiments, the one or more alkenones, one or moreoils (e.g., mono-, di-, and triglycerides), and one or more alcohols caneach independently be present in an amount of from 2% (e.g., from 5%,from 8%, or from 10%) to 15% (e.g., to 10%, to 8%, or to 5%) by weightin the emollient composition. In some embodiments, the emollientcomposition include from 50% (e.g., from 60%, or from 70%) to 80% (e.g.,to 70%, or to 60%) by weight of water. As used herein, it is understoodthat where percentage ranges (e.g., weight percent or volume percent)for components of a composition are provided, the sum of the percentagesof all the components for a specific composition does not exceed 100%.For example, the sum of the percentages of all the components for aspecific composition is 100%.

Cleanser Compositions Including One or More Alkenone or Alkenone-DerivedExfoliant and One or More Surfactant

The accumulation of dead skin cells on the outermost layer of the skincan cause not only undesirable appearance (e.g., dry, dull and flaky),but can also lead to certain skin conditions such as acne. Exfoliationis a process by which the outermost, oldest dead skin cells are removed.Not only does this increase skin softness and appearance, but is alsoimportant for maintaining skin health by encouraging proper cellturnover.

Two types of exfoliants exist: mechanical exfoliants and chemicalexfoliants. Chemical exfoliation (e.g., “chemical peels”) is believed tostimulate new skin cell growth and/or promote dead skin cell lossthrough interactions of the exfoliant compound with certain proteins.See, e.g., Coleman, W. P.; Brody H. J., “Advances in chemical peeling,”Dermatol. Clin. 1997, 15, 19-26. Chemical exfoliation has been reportedfor treatment of serious skin conditions linked to photodamage such asactinic keratosis and other cancers. See, e.g., Rendon, M. I.; Berson,D. S.; Cohen, J. L.; Roberts, W. E.; Starker, I.; Wang, B., “Evidenceand considerations in the application of chemical peels in skindisorders and aesthetic resurfacing,” J. Clin. Aesthet. Dematol. 2010,3, 32-43. These deep exfoliations are specialized treatments withassociated recovery protocols.

Mechanical exfoliation involves the use of abrasives to remove dead skincells on the outermost layer of the skin. This type of exfoliation ismore commonplace with mechanical exfoliating agents found in a varietyof daily-use cleansers. Historically abrasive exfoliants were made frompolyethylene, and their widespread and prolonged use has led to anaccumulation and persistence of these materials. The environmentalimplications of the large amount of microplastics, particularly in themarine environment, are only recently becoming appreciated, as evidencedby a series of recent reports. See, e.g., Napper, I. E.; Bakir, A.;Rowland, S. J.; Thompson, R. C., Marine. Poll. Bull. 2015, 99, pp.178-185, DOI: 10.1016/j.marpolbul.2015.07.029. Eco-friendly exfoliatingagents include ground nut shells and fruit pits. However, thesematerials fail to match the smoothness of polyethylene beads resultingin increased skin irritation.

Alkenones and alkenone derivatives (e.g., alkenones) of the presentdisclosure are waxy solids at room temperature (melting points ˜60-70°C.) with limited solubility in compositions that include surfactants(e.g., soaps). They would therefore exist as solids insurfactant-containing compositions and could serve as gentle mechanicalexfoliants in various cleansers. In some embodiments, alkenone waxeswithin these compositions can form films during cleansing, for instanceas they melt when used with warm water followed by cooling. Formation ofthese waxy films can minimize surfactant skin penetration and theresultant resulting irritation, ideal for sensitive skin products. Thefilms can also provide desirable sheen to, for instance, compositionsfor conditioning hair.

In one embodiment, the composition includes one or more surfactants(e.g., fatty acid carboxylate, sulfates, or betaines); and one or morealkenones and/or alkenone derived compounds of the present disclosure(e.g., alkenones).

The composition can include (exfoliating) skin cleansers or conditioners(e.g., hair). By replacing microplastic abrasives with alkenones, thecomposition could be made from natural components or biodegradablecomponents with significantly reduced environmental impact. Alkenonesand/or alkenone derivatives in these mixtures can also help mitigateirritation and/or provide desirable aesthetic qualities. Using the oilsand soaps from algae along with the alkenones and/or alkenone-derivedcompounds represents a substantive departure from traditionalagricultural plant-based formulations toward more sustainable personalcare compositions.

In some embodiments, an example of an alkenone-containing cleansingcomposition includes one or more alkenones and/or alkenone-derivedcompounds of the present disclosure, one or more oils (e.g., mono-, di-,and triglycerides), one or more fatty surfactants (e.g., sodium laurethsulfate, cocamidopropyl betaine), one or more alcohols (e.g., glycerolor fatty alcohols), and water. In some embodiments, the one or morealkenones and/or alkenone-derived compounds of the present disclosure,one or more oils (e.g., mono-, di-, and triglycerides), one or morefatty surfactants (e.g., sodium laureth sulfate, cocamidopropylbetaine), and one or more alcohols (e.g., glycerol or fatty alcohols)are each independently present in an amount of from 2% (e.g., from 5%,from 10%, from 15%, or from 20%) to 25% (e.g., to 20%, to 15%, to 10%,or to 5%) by weight in the cleansing composition. In some embodiments,the cleansing composition include from 50% (e.g., from 60%, or from 70%)to 80% (e.g., to 70%, or to 60%) by weight of water.

Compositions Including One or More Alkenone-DerivedEmulsifier/Surfactant

Emulsifiers are defined as compounds used to stabilize emulsions, ordispersions of two immiscible substances. Many emulsion-based cosmeticsand personal care products contain emulsifiers to achieve desiredtextural properties and increase product lifetime. Emulsifiers have alsobeen used as delivery vehicles or encapsulating agents to improve theabsorption profiles and bioavailability of various active agents. See,e.g., Souto, E. B.; Severino, P.; Basso, R.; Santana, M. H. A.,“Encapsulation of Antioxidants in Gastrointestinal-ResistantNanoparticulate Carriers,” Oxidative Stress and Nanotechnology: Methodsand Protocols (D. Armstrong and D. J. Bharali, eds.), Springer Science,New York, 2013. The structures of emulsifiers are characterized ascontaining both hydrophilic and hydrophobic (lipophilic) components.

Historically, emulsifier technology was based on petrochemicals such asethylene glycol or mineral oils. For environmental reasons, there hasbeen a shift toward renewable feedstocks. One example is fatty acid(poly)glycerol esters. Glycerol monostearate (GMS) typifies this classof waxy fatty acid emulsifiers, composed of a hydrophilic glycerolcomponent and hydrophobic stearic acid chain (FIG. 5). The physicalproperties and performance of emulsifiers are directly related to thebalance between its hydrophobic and lipophilic groups (HLB value). Inthe case of (poly)glyceryl fatty esters, this would be controlled by thefatty acid carbon chain length and structure (i.e., unsaturationprofile) along with the degree of (poly)glycerol acylation (e.g., mono-,di-, or triglycerides). However, the choice of fatty acid and amountsused in these systems can be constrained by source considerations for aparticular fatty acid. For instance, if the fatty acid is from an animalproduct or a resource intensive (e.g., land and water) edibleagricultural crop.

Incorporation of alkenones, with carbon chain lengths approximatelytwice as long as fatty acids and trans- vs. cis-double bonds, into aglycerol backbone (e.g., a glyceryl monoalkenone (GMA) as shown in FIG.5) can provide lipophilic emulsifiers with unique properties ideallysuited for certain applications. Additionally, compounds from microalgaecan decrease controversies associated with the use of fatty acids fromother feedstocks. It is believed that these alkenone-derived emulsifiersdo not occur in nature.

Most emulsifiers can be considered surfactants, compounds that lower thesurface tension between two immiscible liquids or between a liquid andsolid. It is believed that the degree to which an emulsifier issurface-active is controlled by the HLB. Due to their unique structure,alkenone-derived surfactants would be expected to exhibit different HLBvalues and thus novel properties when compared to current fatty acidbased technologies. Specifically, alkenone surfactants have lower (i.e.,more lipophilic) HLB values than their fatty acid counterpart. This isimportant because for a given formulation, HLB values of the differentingredients (e.g., components A, B and C) are additive:HLB_(mix) =xHLB_(A) +yHLB_(B)+(1-x-y)HLB_(C).Because different compositions can have different specified HLB_(mix)ranges, the incorporation of an alkenone-based surfactant into theseblends can therefore provide a new means for achieving the requisite HLBvalues for these products. Individual alkenone HLB values can also betuned through the incorporation of neutral- (lower HLB) or ionic-headgroups (higher HLB). The lipophilic portion can also be manipulated todiffering carbon chain lengths as outlined in the '460 Application.

Aside from HLB, alkenone-based surfactants can also lend other desirableand superior properties to compositions that include the alkenone-basedsurfactants. For example, skin irritation from cleansing withsurfactants can be caused by the removal of free fatty acids and fattyacid glycerides leading to changes in the intercellular lipid profile.See, e.g., Denda, M.; Koyama, J.; Namba, R. Horii, I., “Stratum corneumlipid morphology and transepidermal water loss in normal skin andsurfactant-induced scaly skin,” Arch. Dermatol. Res. 1994, 286, 41.Moreover, surfactants can penetrate the stratum corneum where they areadsorbed onto proteins (e.g., keratin) and can mix with intracellularlipids. The long hydrocarbon chain of alkenone-based surfactants anddissimilarity with native skin lipids can minimize solubilization (i.e.,fatty acid removal), mixing, and skin penetration of these compounds.Ananthapadmanabhan, K. P.; Moore, D. J.; Subramanyan, K.; Misra, M.;Meyer, F., “Cleansing without compromise: the impact of cleansers on theskin barrier and the technology of mild cleansing,” Dermatologic Ther.2004, 17(s1), 16-25. Aside from improved cleansing performance,alkenone-based surfactants can also lend desirable aesthetic propertiessuch as a desired foaming behavior.

The structures of synthetic alkenone-derived surfactants includes apolar headgroup (“Part A”) and hydrophobic tail (“Part B”, FIG. 5)wherein any group in Part A can be an: alcohol, ester, acid,carboxylate, sulfonate, phosphonate, ammonium or any combinationsthereof. Part B is comprised of an alkenone hydrocarbon chain (35-40carbons, 1-4 trans-double bonds). The dual nature(hydrophobic/hydrophilic) of these derivatives would also make possibletheir use as delivery systems for encapsulating active agents (e.g.,antioxidants). Recalcitrance of alkenones to degradation (see, e.g.,Brassell S. C. (1993), “Applications of biomarkers for delineatingmarine paleoclimatic fluctuations during the Pleistocene,” in OrganicGeochemistry (M. H. Engel and S. A. Macko, eds.), pp. 699-738, PlenumPress, New York) might permit slow release of these active agentsthereby increasing product lifetime in comparison to other traditionalfatty acid-based encapsulation methods. See, e.g., Takahashi, M.;Kitamoto, D.; Asikin, Y.; Takara, K.; Wada, K., “Liposomes EncapsulatingAloe vera Leaf Gel Extract Significantly Enhance Proliferation andCollagen Synthesis in Human Skin Cell Lines,” J. Oleo. Sci. 2009, 58,643-650.

FIG. 6 shows an alkenone-based choline phosphate encapsulation system toenhance active agent (*) delivery. The longer hydrocarbon chain lengthand trans-double bonds of alkenones can provide access to novelsecondary and tertiary structures.

In one embodiment, the encapsulating and/or surfactant compositionincludes one or more alkenone-derived surfactant, one or more mono-,di-, or triglyceride, and one or more alcohol (e.g., glycerol, or fattyalcohol). In some embodiments, one or more alkenone-derived surfactant,one or more mono-, di-, or triglyceride, and one or more alcohol (e.g.,glycerol, or fatty alcohol) can each independently be present in anamount of from 2% (e.g., from 5%, from 8%, or from 10%) to 15% (e.g., to10%, to 8%, or to 5%) by weight in the emollient composition.

The composition can be a soap, a detergent, or a skin cleanser.Alkenone-derived surfactants can be used in mild cleansers (e.g., forinfant care) to decrease skin penetration and irritation, as well asencapsulating active agents for controlled release and to increasebioavailability/stability. Cosmetics with certain textural requirementscan also benefit from alkenone emulsifiers and/or surfactants.

Isolation and Synthesis of Alkenones and Alkenone Derivatives Isolationof Alkenones from Algae

The extraction and/or isolation of alkenones and fatty acids from algalbiomass and their conversion to jet fuel range hydrocarbons andbiodiesel, respectively, has previously been described in the '460Application, the disclosure of which is hereby incorporated by referencein its entirety, along with any publications, patents, or patentapplications cited therein). In the present disclosure, differentcompound sub-classes can be separated to create pools of pure isolatesas outlined in the '460 Application from which optimized personal careformulations can be created. Additionally, pigments can be selectivelyremoved from lipid mixtures to create decolorized compositions withcolors that are better suited to personal care items such as soaps andcreams.

FIG. 7 shows the extraction, processing, separation, and formulation ofalkenone-based topical products from Isochrysis biomass. Dry Isochrysisbiomass 102 is first extracted (e.g., with an organic solvent) toprovide a dark colored alkenone-containing (e.g., around 15% w/w) totallipid extract 104. Green naturally abrasive surfactants can be directlyformed from this product by saponification of acylglycerols along withlighter colored products by removal of pigments (i.e., decolorization)as shown in product 106. Alternatively, purified alkenones 108 can beseparated from polar lipids 110, fatty acids, glycerides, or soaps),derivatized, and reconstituted to specific compositions for optimizedperformance 112.

Alkenone Derivatization

Examples of synthetic alkenone-derived surfactants are outlined in FIG.8. One series is based on the use of reduced alkenones (“alkenols”) toprepare polyoxyethylene derivatives of the alkenones (F), sulfatederivatives of the alkenones (B), ammonium derivatives of the alkenones(H), and betaine (D, E) surface active agents. Others are derived fromoxidized alkenones (alkenoic acids) that would include neutral glycerylemulsifiers. Amino acid derivatives (C) by Strecker synthesis (see,e.g., A. Baeza, C. Nájera, J. M. Sansano, Synthesis, 2007, 1230-1234)can exhibit antimicrobial activities. Referring to FIG. 8, R^(A) ismethyl or ethyl and R^(C) is an alkyl group (C_(n)H_(2n+1), e.g., CH₃).When derived from an alkenone of the present disclosure, R^(B) can be aC₃₂-C₃₇ hydrocarbon chain containing one or more trans-double. Asdescribed in the '460 Application, this R^(B) hydrocarbon chain can bemodified to R^(B)≥C₅ alkene (generally containing one alkene) or C₅alkyl.

Hydrogenation of Alkenones to Alkanones

Alkenones can be hydrogenated to provide alkanones by placing thealkenones under an atmosphere of hydrogen in the presence of a catalyst,such as platinum and/or palladium on carbon. To a solution of alkenonesin ethyl acetate was added palladium on carbon (10% wt Pd, 10% w/walkenones) and the mixture was placed under an atmosphere of hydrogen (1atm.). The reaction was stirred for 6 h before removing the palladium byfiltration through cotton and concentrating the solution in vacuo. Theresulting alkanones were obtained as an off-white solid (98% yield,mp.=55-58° C.).

Reduction of Alkenones to Alkenols

Alkenones can be reduced to the corresponding alkenols by any number ofstandard ketone reduction methods. See, e.g., Modern Reduction Methods(P. G. Andersson, I. J. Munslow, eds.), Wiley-VCH, Weinheim, Germany,2008. The methods generally employ a hydride source ([M]H, where [M] canbe Al, B, Si; e.g., LiAlH₄ or NaBH₄) or the combination of hydrogen anda heterogeneous catalyst (e.g., Pd, Pt, Ni). In a standard reaction,alkenones are dissolved in a mixture of an alcoholic solvent (ROH) andethereal solvent (e.g., tetrahydrofuran) to which is added sodiumborohydride (NaBH₄) and the mixture is stirred for 1 h. The reaction isthen quenched with saturated aq. Brine, and extracted with an organicsolvent (e.g., ethyl acetate, diethyl ether). The organic phase isconcentrated in vacuo to yield the alkenol products that can be usedwithout further purification (yields are generally >90%).

Oxidation of Alkenones to Alkenoic Acids

The oxidation of alkenones to their corresponding carboxylic acids(alkenoic acids) can be accomplished by a variety of classic methodsincluding the haloform reaction (see, e.g., Fuson, R. C.; Bull, B. A.,“The Haloform Reaction,” Chem. Rev. 1934, 15, 275-309), Rubottomoxidation followed by oxidation cleavage (see, e.g., Meinke, P. T.;Colletti, S. L.; Ayer, M. B.; Darkin-Rattray, S. J.; Myers, R. W.;Schmatz, D. M.; Wyvratt, M. J.; Fisher, M. H., Tetrahedron Lett. 2000,41, 7831-7835), or the use of carbon monoxide and water. See, e.g.,Larson, A. T., 1942, “Organic Acids from Ketones,” and U.S. Pat. No.2,273,785. As an example: a solution of alkenones is treated withaqueous sodium hypochlorite (typically 12%=industrial bleach) and themixture is stirred vigorously (generally 1-2 hours). The mixture is thenmade acidic (pH <5) by the addition of HCl. Stirring is stopped and thelayers are allowed to separate. The organic phase containing thealkenoic acids is recovered, dried, and concentrated in vacuo.

Synthesis of Alkenone-Derived Anionic Surfactants

Alkenoic acids can be directly converted to their corresponding anioniccarboxylate surfactants by deprotonation with an appropriate base (e.g.,NaOH or KOH). Other alkenoic acid- or alkenol-derived anionicsurfactants can generally proceed via a condensation or substitutionreaction. For example, sulfate surfactants can be formed by reactions ofalkenols with SO₃·pyridine. In a typical experiment, a solution ofalkenols (10 g) in solvent (e.g., dimethylformamide/dichloromethane(DMF/DCM) mixtures) is treated with pyridine.SO₃ (Pyr·SO₃) (5 g) and themixture is stirred at room temperature for 1-5 h (monitored by thinlayer chromatography (TLC)). Solvent is then removed under reducedpressure to give the corresponding pyridinium alkenol sulfate salt. Toexchange the pyridinium counterion with sodium, the product is treatedwith a sodium alcoholate solvent (e.g., sodium methoxide or sodiumethoxide (NaOMe or NaOEt)) at which point the sodium alkenol sulfate canprecipitate out of solution. The suspension is then centrifuged and thesupernatant removed. Referring to FIG. 8, the product compound B(usually a white powder) can be rinsed (e.g., with methanol) to removetraces of pyridine and dried at 40-50° C. under vacuum (typically 3×10⁻²mbar). Compound purity can be determined by NMR spectroscopy.

Other alkenone-derived sulfates can be synthesized by first condensingan alkenoic acid or alkenol with an appropriate linker (e.g., diol)prior to sulfation. As an example: alkenoic acids can be condensed withan excess of ethylene glycol (typically 3 molar equivalents) in thepresence of acid (e.g., H₂SO₄, approximately 2 mol %) at roomtemperature for approximately 24 h. Neutralization (e.g., with NaHCO₃)followed by portioning with water and an organic solvent (e.g.,dichloromethane) then allows for isolation of the alkenol ethyleneglycol condensation product that can be sulfated according to theprocedure above to yield compound A (FIG. 8).

Synthesis of Alkenone-Derived Betaine Surfactants

Alkenones can be converted to amino acids C by means of Streckerreaction (see, e.g., Strecker, A., “Ueber die künstliche Bildung derMilchsäure und einen neuen, dem Glycocoll homologen Körper,” Annalen derChemie und Pharmazie 1850, 75, 27-45. (b) Strecker, A. (1854). “Uebereinen neuen aus Aldehyd—Ammoniak und Blausäure entstehenden Körper,”Annalen der Chemie und Pharmazie 1854, 91, 349-351) or one of its manyrecent variants. See, e.g., Duthaler, R. O., Tetrahedron 1994, 50,1539-1650 and Shibasaki, M.; Kanai, M.; Mita, K., Org. React. 2008,70, 1. In a standard reaction, alkenones are treated with NaCN (1.0equiv.) in the presence of NH₄Cl (0.5 equiv.) and MgSO₄ (0.5 equiv.) in7M NH₃ in Me0H (3.0 equiv.) at 30° C. for 34. See, e.g., Kuethe, J. T.;Gauthier, D. R.; Beutner, G. L.; Yasuda, N., J. Org. Chem. 2007, 72,7469-7472. Ammonia and methanol (MeOH) are then removed under reducedpressure. Dilution with solvent (e.g., diethyl ether, methyl t-butylether (MTBE), CH₂Cl₂) and removal of the inorganic solids by filtrationthen gives the corresponding amino nitrile that can be hydrolyzed undereither aqueous basic or aqueous acidic conditions.

Betaine surfactants (e.g., D and E, FIG. 8) can be prepared bycondensation of alkenols with an appropriate ammonium phosphonate orammonium carbonate respectively. For the synthesis of D, alkenols aretreated with 2-choloro-1,3,2-dioxaphospholane (1.3 equiv.) in thepresence of trimethylamine (1.75 equiv.). See, e.g., Zhang, Q.; Horst,R.; Geralt, M.; Ma, X.; Hong, W. X.; Finn, M. G.; Stevens, R. C.;Wütrich, K., J. Am. Chem. Soc. 2008, 130, 7357-7363. After 4 h at roomtemperature, triethylammonium chloride is removed by filtration and themixture is concentrated under reduced pressure. The product is thenredissolved in solvent (typically acetonitrile), to which is addedtrimethylamine and the mixture is heated to 70° C. for approximately 48h. Concentration under vacuum then yields the betaine ammoniumphosphonate D.

For the synthesis of E, alkenols are first treated with carbonyldiimidazole (1.1 equiv.) in the presence of ethanediamine (1.3 equiv.).See, e.g., Yoshida, K. I. et al., Bioorg. Med. Chem. 2007, 15,7807-7097. The resulting carbamate is then N-alkylated with tert-butylbromoacetate followed by acidic hydrolysis of the tert-butyl ester togive betaine E.

Synthesis of Alkenol Polyoxyethylene Surfactants

Ethoxylation of alkenols can be carried out by the reaction of alkenolswith ethylene oxide under either basic or Lewis acid catalysis. In atypical reaction, to a solution of alkenols (1 mol) in solvent(tetrahydofuran (THF) or DCM) is added base (e.g., sodium hydride, 0.1mol) followed by ethylene oxide (25 mol). The reaction is quenched withaqueous acid (e.g., 1M HCl) and the product obtained by precipitationfrom solvent. Similarly, sodium or potassium alkenylates can be made toreact with poly(ethyleneglycol)methane sulfonates which can lowerpolydispersity. See, e.g., A. K. Khachadurian, C. H. Fung, T. van Es, F.Davis, Biochim. Biophys. Acta 1981, 665, 434.

Preparation of Alkenone-Derived Cationic Surfactants

Cationic ammonium alkenone derivatives can be made from alkenones viaany number of reductive amination reactions. In a typical procedure,alkenones are dissolved in solvent (e.g., tetrahydrofuran,dichloromethane, or dichloroethane) to which is added an amine (e.g.,dimethylamine (1.0-2.0 equiv.), a reducing agent (e.g., sodiumcyanoborohydride (1.3-1.6 equiv.)) with or without acid (e.g., aceticacid (1.0-2.0 equiv.)). See, e.g., A. F. Abdel-Magid, K. G. Carson, B.D. Harris, C. A. Maryanoff, R. D. Shah, J. Org. Chem., 1996, 61,3849-3862. The mixture is stirred for 0.5-74 hours before quenching withaq. brine and extracting with ethyl acetate or dichloromethane. Theorganic extracts are dried over sodium sulfate, filtered, andconcentrated in vacuo. The resulting alkenamine can then be dissolved intetrahydrofuran and treated with an alkyl halide (e.g., iodomethane(1.0-2.0 equiv.) to generate the corresponding cationic ammoniumcompound.

Alternatively, the ammonium cation can be incorporated through an acyllinker (e.g., compound G, FIG. 8) in analogy to compound E.

Preparation of Alkenone Choline Phosphonate Encapsulating Agents

Glycerol alkenone-based liposomes, nanoemulsions, and lipidnanoparticles can be prepared beginning with monoacylated alkenoic acidderivatives (e.g., GMA). Condensation of GMA with choline phosphate (1.0equiv.) in refluxing ethanol (˜85° C.) would provide the monoalkenonemonocholine phosphonate adduct.

Alternatively, alkenones can be coupled with choline alfoscerate. In atypical reaction, to a solution of alkenones (1.0 equiv.) and cholinealfoscerate (2-4 equiv.) in CH₂Cl₂ was added dicyclohexylcarbodiimide(DCC, 1.1 equiv.) followed by catalytic dimethylaminopyridine (DMAP,3-10 mol %) and the mixture was stirred for 24-72 h. See, e.g., Neises,B.; Steglich, W., Angew. Chem. Int. Ed. 1978, 17, 522-524. The ratio ofalkenones to choline alfoscerate can be manipulated to select for theformation of mono- or di-alkenone choline phosphates. Fatty acids canalso be introduced in this manner with or without isolation ofmonoalkenone choline phosphate to produce alkenone/fatty acid cholinephosphate hybrids.

Preparation of Compositions Preparation of Alkenone-Based Abrasive Soaps

Treatment of algal oil with KOH or NaOH at 60° C. results insaponification of the acylglycerols as described in the '460Application. The resulting mixture generally contains approximately 50%w/w soap, with the remainder being primarily alkenones (˜15% w/w) andpigments such as chlorophylls. Pigments can be removed by decolorizationwith an adsorbent as described above, pre- or post-saponification toyield a light yellow-colored soap/alkenone mixture. Alternatively,isolated alkenones and soaps can be recombined to provide specificalkenone/soap compositions of varying concentrations (e.g., 10-50% w/walkenones). Alkenone solubility in these mixtures is <1 mg/mL, so thesecompounds remain as waxy solids.

Preparation of Alkenone Cleansers

Compositions can be made by combining isolated (and decolorized)alkenones with surfactants to provide exfoliating skin care products.

Preparation of Alkenone-Containing Skin-Care Products

Compositions can be made directly made from the algal oil containingprimarily acylglycerols (approximately 40%) along with alkenones(approximately 10%) and pigments like chlorophylls and carotenoids.Decolorization of this material using similar technology to thatdescribed for the alkenones would provide a yellow-colored compositionwith elevated triglyceride (50-60%) and alkenone (15-20%) contents.Compositions can also be prepared starting with isolated (and if desireddecolorized) alkenones. Depending on their intended use (e.g., cream,ointment, paste, lotion, gel), other ingredients can include, forexample, water, oils, hydrocarbons, alcohols, free fatty acids plusemulsifiers, thickening agents, and preservatives.

The following examples are provided to illustrate, not limit, theinvention.

Example 1 describes extraction and purification of alkenones frommicroalgae of the lipids. Example 2 describes the hydrogenation ofalkenones to alkenones. Example 3 describes the reduction of alkenonesto alkenols. Example 4 describes oxidation of alkenones to alkenoicacids. Example 5 describes the synthesis of alkenone-derived anionicsurfactants. Example 6 describes the synthesis of alkenone-derivedbetaine surfactants. Example 7 describes the synthesis of alkenolpolyoxyethylene surfactants. Example 8 describes the preparation ofalkenone-derived cationic surfactants. Example 9 describes thepreparation of alkenone choline phosphonate encapsulating agents.

EXAMPLES Example 1 Microalgae and Extraction of Alkenones

Algae are processed and the lipids extracted according to methodsdescribed in the '460 Application. As a specific example, dry Isochrysisbiomass is extracted by Soxhlet using hexanes as solvent to provide analgal oil containing approximately 50% w/w fatty acid derivatives (e.g.,acylglycerols) and 15% w/w alkenones. An exemplary alkenone profile ofthis material is presented in Table 2. See, e.g., O'Neil, G. W.;Carmichael, C. A.; Goepfert, T. J.; Fulton, J. M.; Knothe, G.; Lau, C.P. L.; Lindell, S. R.; Mohammady, N. G. E.; Van Mooy, B. A. S.; Reddy,C. M., “Beyond Fatty Acid Methyl Esters: Expanding the Renewable CarbonProfile with Alkenones from Isochrysis sp.” Energy Fuels 2012, 26,2434-2441.

TABLE 2 Typical alkenone composition of Isochrysis sp. mg/g ofIsochrysis sp. mg/g of dry weight of Alkenones algal oil Isochrysis sp.Me 37:3 (8E, 15E, 22E) 67 13 Me 37:2 (15E, 22E) 43 9 Et 38:3 (9E, 16E,23E) 8 2 Et 38:2 (9E, 16E, 23E) 37 7 Me 39:3 (8E, 15E, 22E) 2 1 Me 39:2(15E, 22E) 4 1 Total Alkenones 161 33

Separation of Neutral and Polar Lipids

Alkenones and other neutral lipids can be separated from polar lipids(e.g., fatty acids) contained in the algal oil by treatment with KOH orNaOH at 60° C. as described in the '460 Application. The resultingsaponified acylglycerols (i.e. soaps) can be partitioned into waterwhile neutral lipids are extracted with an organic solvent (typicallyhexanes). Mass balance is generally 40% neutral lipids.

Recovery of Free Fatty Acids

Reacidification of aqueous soap mixtures with HCl produces thecorresponding free fatty acids. These can then be extracted with anorganic solvent such as hexanes. Mass recoveries of free fatty acids istypically 60% w/w from the algal oil.

Isolation and Purification of Alkenones From the Neutral Lipids

Alkenones can be isolated and purified from the neutral lipids asdescribed in the '460 Application by chromatography on silica andrecrystallization (FIG. 1C).

Decolorization of Alkenones

Brilliant white alkenones (i.e., purified alkenones 108 of FIG. 7) thatcan be preferred for certain applications can be obtained bydecolorization using various solid materials such as clays or activatedcarbon based on technology used in vegetable oil refining. In a typicalprocedure, to the neutral lipids (10 g, pre- or post-silicachromatography) in hexanes (50 mL) at 60° C. was added the acidic claymontmorillonite K 10 (1 g) and the mixture was stirred for 3 h. Thereaction was hot-filtered to remove the MK10, and upon cooling to roomtemperature alkenones (typically 4 g) crystallized out of solution. Thisprocedure can be repeated as necessary to achieve the desired level ofdecolorization.

Example 2 Hydrogenation of Alkenones to Alkanones

To a solution of alkenones in ethyl acetate was added palladium oncarbon (10% wt Pd, 10% w/w alkenones) and the mixture was placed underan atmosphere of hydrogen (1 atm.). The reaction was stirred for 6 hbefore removing the palladium by filtration through cotton andconcentrating the solution in vacuo. The resulting alkanones wereobtained as an off-white solid (98% yield, mp.=55-58° C.).

Example 3 Reduction of Alkenones to Alkenols

In a standard reaction, alkenones are dissolved in a mixture of analcoholic solvent (ROH) and ethereal solvent (e.g., tetrahydrofuran) towhich is added sodium borohydride (NaBH₄) and the mixture is stirred for1 h. The reaction is then quenched with saturated aq. Brine, andextracted with an organic solvent (e.g., ethyl acetate, diethyl ether).The organic phase is concentrated in vacuo to yield the alkenol productsthat can be used without further purification (yields aregenerally >90%). Referring to FIG. 9, the reduction of alkenones toalkenols can be observed by the loss of the C═O stretch at about 1711cm-1 and emergence of a new O—H stretch in an infrared spectrum

Example 4 Oxidation of Alkenones to Alkenoic Acids

A solution of alkenones is treated with aqueous sodium hypochlorite(typically 12%=industrial bleach) and the mixture is stirred vigorously(generally 1-2 hours). The mixture is then made acidic (pH<5) by theaddition of HCl. Stirring is stopped and the layers are allowed toseparate. The organic phase containing the alkenoic acids is recovered,dried, and concentrated in vacuo.

Example 5 Synthesis of Alkenone-Derived Anionic Surfactants

A solution of alkenols (10 g) in solvent (e.g., DMF/DCM mixtures) istreated with Pyr.SO₃ (5 g) and the mixture is stirred at roomtemperature for 1-5 h (monitored by TLC). Solvent is then removed underreduced pressure to give the corresponding pyridinium alkenol sulfatesalt. To exchange the pyridinium counterion with sodium, the product istreated with a sodium alcoholate solvent (e.g., NaOMe or NaOEt) at whichpoint the sodium alkenol sulfate can precipitate out of solution. Thesuspension is then centrifuged and the supernatant removed. The productcompound B (FIG. 8, usually a white powder) can be rinsed (e.g., withmethanol) to remove traces of pyridine and dried at 40-50° C. undervacuum (typically 3×10⁻² mbar). Compound purity can be determined by NMRspectroscopy.

Alkenone-derived anionic surfactants of structure A (FIG. 8) can be madeby condensing alkenoic acids with an excess of ethylene glycol(typically 3 molar equivalents) in the presence of acid (e.g., H₂SO₄,approximately 2 mol %) at room temperature for approximately 24 h.Neutralization (e.g., with NaHCO₃) followed by portioning with water andan organic solvent (e.g., dichloromethane) then allows for isolation ofthe alkenol ethylene glycol condensation product that can be sulfatedaccording to the procedure above to yield compound A.

Example 6 Synthesis of Alkenone-Derived Betaine Surfactants

Alkenones are treated with NaCN (1.0 equiv.) in the presence of NH₄Cl(0.5 equiv.) and MgSO₄ (0.5 equiv.) in 7M NH₃ in MeOH (3.0 equiv.) at30° C. for 34. See, e.g., Kuethe, J. T.; Gauthier, D. R.; Beutner, G.L.; Yasuda, N., J. Org. Chem. 2007, 72, 7469-7472. Ammonia and MeOH arethen removed under reduced pressure. Dilution with solvent (e.g.,diethyl ether, MTBE, CH₂Cl₂) and removal of the inorganic solids byfiltration then gives the corresponding amino nitrile that can behydrolyzed under either aqueous basic or aqueous acidic conditions toprovide C (FIG. 8).

Betaine surfactants (e.g., D and E, FIG. 8) can be prepared bycondensation of alkenols with an appropriate ammonium phosphonate orammonium carbonate respectively. For the synthesis of D, alkenols aretreated with 2-choloro-1,3,2-dioxaphospholane (1.3 equiv.) in thepresence of trimethylamine (1.75 equiv.). After 4 h at room temperature,triethylammonium chloride is removed by filtration and the mixture isconcentrated under reduced pressure. The product is then redissolved insolvent (typically acetonitrile), to which is added trimethylamine andthe mixture is heated to 70° C. for approximately 48 h. Concentrationunder vacuum then yields the betaine ammonium phosphonate D.

For the synthesis of E, alkenols are first treated with carbonyldiimidazole (1.1 equiv.) in the presence of ethanediamine (1.3 equiv.).The resulting carbamate is then N-alkylated with tert-butyl bromoacetatefollowed by acidic hydrolysis of the tert-butyl ester to give betaine E.

Example 7 Synthesis of Alkenol Polyoxyethylene Surfactants

To a solution of alkenols (1 mol) in solvent (THF or DCM) is added base(e.g., sodium hydride, 0.1 mol) followed by ethylene oxide (25 mol). Thereaction is quenched with aqueous acid (e.g., 1M HCl) and the productobtained by precipitation from solvent. Similarly, sodium or potassiumalkenylates can be made to react with poly(ethyleneglycol)methanesulfonates which can lower polydispersity.

Example 8 Preparation of Alkenone-Derived Cationic Surfactants

Alkenones are dissolved in solvent (e.g., tetrahydrofuran,dichloromethane, or dichloroethane) to which is added an amine (e.g.,dimethylamine (1.0-2.0 equiv.), a reducing agent (e.g., sodiumcyanoborohydride (1.3-1.6 equiv.)) with or without acid (e.g., aceticacid (1.0-2.0 equiv.)). The mixture is stirred for 0.5-74 hours beforequenching with aq. brine and extracting with ethyl acetate ordichloromethane. The organic extracts are dried over sodium sulfate,filtered, and concentrated in vacuo. The resulting alkenamine can thenbe dissolved in tetrahydrofuran and treated with an alkyl halide (e.g.,iodomethane (1.0-2.0 equiv.) to generate the corresponding cationicammonium compound.

Alternatively, the ammonium cation can be incorporated through an acyllinker (e.g., compound G, FIG. 8) in analogy to compound E.

Example 9 Preparation of Alkenone Choline Phosphonate EncapsulatingAgents

Glycerol alkenone-based liposomes, nanoemulsions, and lipidnanoparticles can be prepared beginning with monoacylated alkenoic acidderivatives (e.g., GMA). Condensation of GMA with choline phosphate (1.0equiv.) in refluxing ethanol (˜85° C.) would provide the monoalkenonemonocholine phosphonate adduct.

Alternatively alkenones can be coupled with choline alfoscerate: to asolution of alkenones (1.0 equiv.) and choline alfoscerate (2-4 equiv.)in CH₂Cl₂ was added dicyclohexylcarbodiimide (DCC, 1.1 equiv.) followedby catalytic dimethylaminopyridine (DMAP, 3-10 mol %) and the mixturewas stirred for 24-72 h. The ratio of alkenones to choline alfosceratecan be manipulated to select for the formation of mono- or di-alkenonecholine phosphates. Fatty acids can also be introduced in this mannerwith or without isolation of monoalkenone choline phosphate to producealkenone/fatty acid choline phosphate hybrids.

The embodiments of the invention in which an exclusive property orprivilege is claimed are defined as follows:
 1. A personal carecomposition, comprising: a compound of Formula (I):

wherein R₁ is methyl or ethyl; and R₂ is a C₃₀₋₄₅ alkenyl having atleast one trans double carbon-carbon bond, or R₂ is a C₃₀₋₄₅ alkyl;provided that the compound of Formula (I) is not

wherein the composition does not comprise carotenoids and chlorophylls,and the composition does not comprise a total algae lipid extract or anacylglycerol.
 2. The personal care composition of claim 1, furthercomprising a synthetic agent selected from synthetic solubilizingagents, synthetic emulsifying agents, synthetic humectants, syntheticemollients, synthetic occlusive agents, synthetic surfactants, syntheticpreservatives, synthetic binding agents, synthetic thickeners, syntheticsolvents, synthetic fragrances, and any combination thereof.
 3. Thepersonal care composition of claim 1, further comprising a naturallyoccurring agent selected from natural emollients, natural occlusiveagents, natural emulsifying agents, natural anti-oxidants, naturalcolorants, natural fragrances, and any combination thereof.
 4. Thepersonal care composition of claim 1, wherein R₂ is a C₃₅₋₄₅ alkenylhaving at least one trans double carbon-carbon bond.
 5. The personalcare composition of claim 1, wherein R₂ has 2 to 4 trans doublecarbon-carbon bonds.
 6. The personal care composition of claim 1,wherein the compound of Formula (I) is selected from the groupconsisting of:

wherein R₁ is methyl or ethyl, and R_(2-C34) is C₃₄ alkenyl having 2 or3 trans double carbon-carbon bonds;

wherein R₁ is methyl or ethyl, and R_(2-C35) is C₃₅ alkenyl having 2 or3 trans double carbon-carbon bonds;

wherein R₁ is methyl or ethyl, and R_(2-C36) is C₃₆ alkenyl having 2 or3 trans double carbon-carbon bonds;

wherein R₁ is methyl or ethyl, and R_(2-C37) is C₃₇ alkenyl having 1, 2,3, or 4 trans double carbon-carbon bonds;

wherein R₁ is methyl or ethyl, and R_(2-C38) is C₃₈ alkenyl having 1, 2,3, or 4 trans double carbon-carbon bonds; and

wherein R₁ is methyl or ethyl and R_(2-C39) is C₃₉ alkenyl having 1, 2,3, or 4 trans double carbon-carbon bonds.
 7. The personal carecomposition of claim 1, wherein R₂ has two or more trans doublecarbon-carbon bonds, and at least two of the trans double carbon-carbonbonds are spaced from one another by 5 carbon atoms.
 8. The personalcare composition of claim 1, wherein the composition is in the form of atopical formulation.
 9. The personal care composition of claim 1,wherein the composition is selected from the group consisting of askin-care composition, a hair-care composition, and a cosmeticcomposition.
 10. The personal care composition of claim 1, wherein thecompound of formula (I) is a waxy solid at room temperature and presentfrom 1-50% w/w of the total composition.
 11. The personal carecomposition of claim 1, wherein the compound of formula (I) is derivedfrom algae selected from the group consisting of Isochrysis, Emilianiahuxleyi, and Gephyrocapsa oceanica.
 12. The personal care composition ofclaim 1, wherein the composition does not include any petroleum-basedwaxes or oils, plant-based fats, animal-based fats, or any combinationthereof.
 13. The personal care composition of claim 1, wherein thecompound of formula (I) is present in an amount of from 5% to 35% w/w ofthe total composition.
 14. The personal care composition of claim 1,wherein the compound of formula (I) is present in an amount of from 10%to 35% w/w of the total composition.
 15. The personal care compositionof claim 1, wherein the compound of formula (I) is present in an amountof from 2% to 15% w/w of the total composition.
 16. The personal carecomposition of claim 1, wherein the compound of formula (I) is presentin an amount of from 5% to 15% w/w of the total composition.
 17. Apersonal care composition, comprising: an algal extract consisting of acompound of Formula (I):

wherein R₁ is methyl or ethyl; and R₂ is a C₃₀₋₄₅ alkenyl having atleast one trans double carbon-carbon bond, or R₂ is a C₃₀₋₄₅ alkyl;provided that the compound of Formula (I) is not

wherein the composition does not comprise carotenoids and chlorophylls,and the composition does not comprise a total algae lipid extract or anacylglycerol.